PharmaZell
NDC Database
PharmaZell
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 51
- Latest Marketing Date 2025-11-12
- Data Source FDA
- First Marketing Date 1989-05-09
Company Overview
Social Profiles
Company Snapshot
PharmaZell
Headquarters, HochstraB-Süd 7, 83064 Raubling
Germany
www.axplora.com axplora@axplora.com View on MapNDC Records ( 51 records )
Nonproprietary Name
Prucalopride succinate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
PRUCALOPRIDE SUCCINATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalazine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalazine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalazine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalazine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalazine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1989-05-09
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1989-05-09
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Balsalazide Disodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
BALSALAZIDE DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2004-08-05
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Propafenone hydrochloride
Dosage Form
POWDER
Strength
1 h/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
PROPAFENONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1992-12-16
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Propafenone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
PROPAFENONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Propafenone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
PROPAFENONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Propafenone hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
PROPAFENONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Propafenone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
PROPAFENONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Propafenone Hydrochloride
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
PROPAFENONE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Propafenone
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
PROPAFENONE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalazine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2001-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Carbocisteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
CARBOCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2011-04-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Carbocisteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
CARBOCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1997-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
L-Leucine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
LEUCINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Balsalazide Disodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
BALSALAZIDE DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-07-09
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Balsalazide Disodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
BALSALAZIDE DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Balsalazide Disodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
BALSALAZIDE DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Balsalazide Disodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
BALSALAZIDE DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-07-09
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Balsalazide Disodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
BALSALAZIDE DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Balsalazide Disodium
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
BALSALAZIDE DISODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
L-Cystine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
CYSTINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2008-08-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Acetylcysteine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
ACETYLCYSTEINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1995-01-01
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-12-25
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2021-10-09
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2017-07-12
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-06-18
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
GUANFACINEHYDROCHLORIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
GUANFACINE HYDROCHLORIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-03-31
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Celecoxib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
CELECOXIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-11-25
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Celecoxib
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
CELECOXIB
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-11-25
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Methylene blue
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
METHYLENE BLUE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2018-01-08
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-04-03
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Mesalamine
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
MESALAMINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2016-04-03
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Cholic acid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
CHOLIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-08-27
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Cholic acid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
CHOLIC ACID
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2024-08-27
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Chenodeoxycholic acid
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
PharmaZell GmbH
Marketing Category
BULK INGREDIENT
Substance
CHENODIOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2025-11-12
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
51 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).
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NDC
12598-5142
Nonproprietary Name
Prucalopride succinate
Labeler
PharmaZell GmbH
Dosage Form
POWDER
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