PCAS
NDC Database
PCAS
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 17
- Latest Marketing Date 2026-03-01
- Data Source FDA
- First Marketing Date 2009-08-14
Company Overview
Social Profiles
Company Snapshot
PCAS
21, chemin de la sauvegarde 69134, Ecully Cedex
France
www.pcas.com/ PAPI@seqens.com View on MapNDC Records ( 17 records )
Nonproprietary Name
METHYLNALTREXONE BROMIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
METHYLNALTREXONE BROMIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-10-01
End Marketing Date
2029-07-29
Listing Record Certified Through
-
Nonproprietary Name
PINDOLOL
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
PINDOLOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-08-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
OXYBUTYNIN CHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
OXYBUTYNIN CHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-10-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
PRAZIQUANTEL
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
PRAZIQUANTEL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-07-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
VEDAPROFEN
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
VEDAPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-07-07
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
CICLOPIROX OLAMINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
CICLOPIROX OLAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-07-07
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Clomiphene Citrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
CLOMIPHENE CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-11-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
KETAMINE HYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
KETAMINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2024-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ENCLOMIPHENE CITRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
ENCLOMIPHENE CITRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-10-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
BUPRENORPHINE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
BUPRENORPHINE
Product Type
BULK INGREDIENT
DEA Schedule
CIII
Start Marketing Date
2026-03-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
VALPROIC ACID
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
VALPROIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-23
End Marketing Date
2029-07-31
Listing Record Certified Through
-
Nonproprietary Name
MIFEPRISTONE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
MIFEPRISTONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-18
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Divalproex Sodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
DIVALPROEX SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2009-12-18
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Troxerutine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
TROXERUTIN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-02-25
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mipri
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
MIFEPRISTONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-01-28
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Roluperidone HCl
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
ROLUPERIDONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-11-22
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
SODIUM PHENYLBUTYRATE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PCAS
Marketing Category
BULK INGREDIENT
Substance
SODIUM PHENYLBUTYRATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
NDC Type Breakdown
17 total- Bulk Ingredient
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
Explore important National Drug Code information available in the records above.
NDC
10577-919
Nonproprietary Name
METHYLNALTREXONE BROMIDE
Labeler
PCAS
Dosage Form
POWDER
FDA NDC Data
National Drug Code information
Regular Updates
Data maintained from official sources
Structured Database
Searchable pharmaceutical data
Reliable Data
Organized NDC records
Create a New Buying Request
Fields marked with * are mandatory.