Mallinckrodt Pharmaceuticals
NDC Database
Mallinckrodt Pharmaceuticals
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 102
- Latest Marketing Date 2025-08-28
- Data Source FDA
- First Marketing Date 1973-06-30
Company Overview
Company
Mallinckrodt Pharmaceuticals
Country
Ireland
Website
Social Profiles
Company Snapshot
Mallinckrodt Pharmaceuticals
College Business & Technology Park Cruiserath, Blanchardstown Dublin 15
Ireland
www.mallinckrodt.com/ simon.plevin@mnk.com View on MapNDC Records ( 102 records )
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acetaminophen Anhydrous Basis
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
1982-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acetaminophen Anhydrous Basis
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
1982-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ACETAMINOPHEN ANHYDROUS BASIS
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acetaminophen Anhydrous Basis And Chlorpheniramine Maleate
Dosage Form
POWDER
Strength
.9; .0055 kg/kg; kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
FENTANYL ALKALOID
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
FENTANYL
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
1994-09-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acetaminophen Anhydrous Basis
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
1982-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acetaminophen Anhydrous Basis
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Lisdexamfetamine Dimesylate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
LISDEXAMFETAMINE DIMESYLATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2020-05-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SUFENTANIL
Dosage Form
POWDER
Strength
1 g/g
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
SUFENTANIL
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SUFENTANIL
Dosage Form
POWDER
Strength
1 g/g
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
SUFENTANIL
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
LEVORPHANOL TARTRATE
Dosage Form
POWDER
Strength
1 g/g
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
LEVORPHANOL TARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
METHYLPHENIDATE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
METHYLPHENIDATE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2014-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SUFENTANIL CITRATE
Dosage Form
POWDER
Strength
1 g/g
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
SUFENTANIL CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sufentanil Citrate
Dosage Form
POWDER
Strength
1 g/g
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
SUFENTANIL CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2017-01-27
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2023-07-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Oxymorphone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
OXYMORPHONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2010-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acetaminophen Anhydrous Basis
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
1982-12-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dexmethylphenidate Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DEXMETHYLPHENIDATE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2016-08-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Dosage Form
TABLET
Strength
325; 5 mg/1; mg/1
Labeler
SpecGx LLC
Marketing Category
EXPORT ONLY
Substance
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
CII
Start Marketing Date
2022-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Dosage Form
TABLET
Strength
325; 7.5 mg/1; mg/1
Labeler
SpecGx LLC
Marketing Category
EXPORT ONLY
Substance
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
CII
Start Marketing Date
2022-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
Dosage Form
TABLET
Strength
325; 10 mg/1; mg/1
Labeler
SpecGx LLC
Marketing Category
EXPORT ONLY
Substance
ACETAMINOPHEN; HYDROCODONE BITARTRATE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
CII
Start Marketing Date
2022-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fentanyl Citrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
FENTANYL CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
1996-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
FENTANYL CITRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
FENTANYL CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
METHYLNALTREXONE BROMIDE
Dosage Form
POWDER
Strength
50 kg/50kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
METHYLNALTREXONE BROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fentanyl Citrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
FENTANYL CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-11-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
METHYLPHENIDATE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
METHYLPHENIDATE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2014-03-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nalmefene Base
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NALMEFENE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
FENTANYL CITRATE
Dosage Form
POWDER
Strength
20 kg/20kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
FENTANYL CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
naltrexone hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NALTREXONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-04-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
NALOXONE HYDROCHLORIDE DIHYDRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NALOXONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naloxone HCl Ultra Fine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NALOXONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-11-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Methadone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
METHADONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2012-04-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
MORPHINE SULFATE
Dosage Form
POWDER
Strength
95 kg/95kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
MORPHINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Cocaine Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
COCAINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-12-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Morphine Sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
MORPHINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
1977-12-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CODEINE PHOSPHATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
CODEINE PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
1973-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Codeine Phosphate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
CODEINE PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
1986-12-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
HYDROCODONE BITARTRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
HYDROCODONE BITARTRATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2011-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Codeine Phosphate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
CODEINE PHOSPHATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
1975-08-15
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CODEINE SULFATE
Dosage Form
POWDER
Strength
95 kg/95kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
CODEINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
meperidine hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
MEPERIDINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-11-20
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Diphenoxylate Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DIPHENOXYLATE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-11-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
diphenoxylate hydrochloride
Dosage Form
POWDER
Strength
.01; .99 kg/kg; kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
CV
Start Marketing Date
2013-04-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
dextroamphetamine sulfate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DEXTROAMPHETAMINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-29
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
DEXTROAMPHETAMINE SACCHARATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DEXTROAMPHETAMINE SACCHARATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-11-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen anhydrous basis
Dosage Form
POWDER
Strength
0.95 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUPRENORPHINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
BUPRENORPHINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2011-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUPRENORPHINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
BUPRENORPHINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2011-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUPRENORPHINE BASE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
BUPRENORPHINE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2011-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUPRENORPHINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
BUPRENORPHINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2011-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
HYDROMORPHONE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
HYDROMORPHONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2011-12-17
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
NALBUPHINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NALBUPHINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
IBUPROFEN
Dosage Form
POWDER
Strength
0.63 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
IBUPROFEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ibuprofen
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
IBUPROFEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Acetaminophen Anhydrous Basis / Paracetamol Ph Eur
Dosage Form
POWDER
Strength
0.97 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Naltrexone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NALTREXONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-06-06
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
PARACETAMOL
Dosage Form
POWDER
Strength
0.96 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PARACETAMOL
Dosage Form
POWDER
Strength
0.96 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
AMPHETAMINE ASPARTATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
AMPHETAMINE ASPARTATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-11-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
0.95 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-13
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PARACETAMOL
Dosage Form
POWDER
Strength
0.955 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
AMPHETAMINE SULFATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
AMPHETAMINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-11-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Fentanyl Alkaloid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
FENTANYL
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2001-12-21
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Nalmefene Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NALMEFENE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-03-03
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Noscapine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NOSCAPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-12-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Noscapine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
NOSCAPINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-12-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-08-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ACETAMINOPHEN ANHYDROUS BASIS
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2013-02-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Paracetamol
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2020-07-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ACETAMINOPHEN ANHYDROUS BASIS
Dosage Form
POWDER
Strength
0.9 kg/kg
Labeler
SpecGx LLC
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ACETAMINOPHEN
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
1997-09-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
METHYLPHENIDATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
METHYLPHENIDATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
acetaminophen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
ACETAMINOPHEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-02-19
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextromethadone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
METHADONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2025-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextromethadone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
METHADONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2025-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
OXYCODONE HYDROCHLORIDE D
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
OXYCODONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
1986-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
OXYCODONE HCL LOW - ALPHA BETA UNSATURATED KETONE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
OXYCODONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2008-06-30
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextroamphetamine Base
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DEXTROAMPHETAMINE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2013-04-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Methadone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
METHADONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2014-06-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Methadone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
METHADONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2014-06-09
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextroamphetamine Saccharate NP
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DEXTROAMPHETAMINE SACCHARATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2025-08-28
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Dextroamphetamine Saccharate Fine NP
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DEXTROAMPHETAMINE SACCHARATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2025-08-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextroamphetamine Sulfate NP
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DEXTROAMPHETAMINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2025-08-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Dextroamphetamine Sulfate Fine NP
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
SpecGx LLC
Marketing Category
BULK INGREDIENT
Substance
DEXTROAMPHETAMINE SULFATE
Product Type
BULK INGREDIENT
DEA Schedule
CII
Start Marketing Date
2025-08-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
102 total- Bulk Ingredient
- Drug for Further Processing
Official Source
NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).
Visit FDA NDC DirectoryNDC Record Details Preview
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NDC
0406-0046
Nonproprietary Name
acetaminophen
Labeler
SpecGx LLC
Dosage Form
POWDER
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