National Drug Code (NDC) Database
Piramal Pharma Solutions Inc.
-
NDC:
58621-011
-
Nonproprietary Name:
Cetirizine Hydrochloride
-
Dosage Form:
INJECTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 mg/mL
-
Substance:
CETIRIZINE HYDROCHLORIDE
-
Start Marketing Date:
2025-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Pisgah Laboratories, Inc
-
NDC:
63804-0016
-
Nonproprietary Name:
8-((4-amino-1-methylbutyl) amino)-6-methoxyquinoline phosphate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
13 kg/13kg
-
Substance:
PRIMAQUINE PHOSPHATE
-
Start Marketing Date:
2019-03-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Pisgah Labs, Incorporated
-
NDC:
63804-0024
-
Nonproprietary Name:
Etomidate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
33 kg/33kg
-
Substance:
ETOMIDATE
-
Start Marketing Date:
2005-03-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
PLD Acquisitions LLC DBA Avéma Pharma Solutions
-
NDC:
63548-9731
-
Nonproprietary Name:
Prilosec Omeprazole
-
Dosage Form:
TABLET, DELAYED RELEASE
-
Product Type:
BULK INGREDIENT
-
Strength:
20 mg/1
-
Substance:
OMEPRAZOLE
-
Start Marketing Date:
2025-04-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Pliva Croatia Ltd
-
NDC:
11722-064
-
Nonproprietary Name:
Etodolac Micronized
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 kg/100kg
-
Substance:
ETODOLAC
-
Start Marketing Date:
2017-01-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
POET Biorefining - Leipsic, LLC
-
NDC:
81367-001
-
Nonproprietary Name:
Ethanol
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1000 L/1000L
-
Substance:
ALCOHOL
-
Start Marketing Date:
2021-01-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
POLPHARMA BIOLOGICS SA
-
NDC:
82775-100
-
Nonproprietary Name:
ranibizumab
-
Dosage Form:
SOLUTION, CONCENTRATE
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
RANIBIZUMAB
-
Start Marketing Date:
2022-06-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
63804-0019
-
Nonproprietary Name:
Tapentadol Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TAPENTADOL HYDROCHLORIDE
-
Start Marketing Date:
2024-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2026-12-31
-
NDC:
72091-050
-
Nonproprietary Name:
Loratadine
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 mg/1
-
Substance:
LORATADINE
-
Start Marketing Date:
2026-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
49632-180
-
Nonproprietary Name:
ECONAZOLE NITRATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ECONAZOLE NITRATE
-
Start Marketing Date:
2015-10-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Create a New Buying Request
Fields marked with * are mandatory.