BASF
NDC Database
BASF
NDC Database
National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.
- Total Records 24
- Latest Marketing Date 2022-05-01
- Data Source FDA
- First Marketing Date 1980-01-01
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BASF
Carl-Bosch-Strasse 38 Ludwigshafen , Rhineland-Palatinate 67056
Germany
pharmaceutical.basf.com/global/en.html global.info@basf.com View on MapNDC Records ( 24 records )
Nonproprietary Name
Poloxalene
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
POLOXALENE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1980-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ibuprofen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
IBUPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ibuprofen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
IBUPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
IBUPROFEN DC85W
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
IBUPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-01-02
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Ibuprofen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Substance
IBUPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-08
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Ibuprofen
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
IBUPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-06-08
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Sodium Ibuprofen Dihydrate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
IBUPROFEN SODIUM
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2005-04-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Poloxalene
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
POLOXALENE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1980-01-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zinc Oxide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
ZINC OXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-05-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zinc Oxide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
ZINC OXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2000-05-25
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zinc Oxide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
ZINC OXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-08-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zinc Oxide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
ZINC OXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2012-05-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zinc Oxide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
ZINC OXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-05-12
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
ZINC OXIDE
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
ZINC OXIDE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2019-03-31
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zinc Oxide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
ZINC OXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2019-05-06
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Zinc Oxide
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
ZINC OXIDE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2022-05-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Octinoxate, Avobenzone
Dosage Form
LIQUID
Strength
1; 1 kg/kg; kg/kg
Labeler
BASF Corporation
Marketing Category
DRUG FOR FURTHER PROCESSING
Substance
AVOBENZONE; OCTINOXATE
Product Type
DRUG FOR FURTHER PROCESSING
DEA Schedule
Start Marketing Date
2005-01-14
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Kollisolv PEG 3350
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
POLYETHYLENE GLYCOL 3350
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2007-10-03
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
PVP Iodine 30/60
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF Corporation
Marketing Category
BULK INGREDIENT
Substance
POVIDONE-IODINE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2010-01-11
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Menthol Pharma
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF SE
Marketing Category
BULK INGREDIENT
Substance
LEVOMENTHOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-07-01
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
L-Menthol Pharma Flakes
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF SE
Marketing Category
BULK INGREDIENT
Substance
LEVOMENTHOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2014-09-22
End Marketing Date
-
Listing Record Certified Through
2027-12-31
Nonproprietary Name
Dexpanthenol
Dosage Form
SYRUP
Strength
1 kg/kg
Labeler
BASF SE
Marketing Category
BULK INGREDIENT
Substance
DEXPANTHENOL
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2015-06-26
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Racemic Ibuprofen Lysinate
Dosage Form
POWDER
Strength
1 kg/kg
Labeler
BASF SE
Marketing Category
BULK INGREDIENT
Substance
IBUPROFEN
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
2013-09-10
End Marketing Date
-
Listing Record Certified Through
2026-12-31
Nonproprietary Name
Octinoxate
Dosage Form
LIQUID
Strength
1 kg/kg
Labeler
BASF SE
Marketing Category
BULK INGREDIENT
Substance
OCTINOXATE
Product Type
BULK INGREDIENT
DEA Schedule
Start Marketing Date
1999-05-17
End Marketing Date
-
Listing Record Certified Through
2027-12-31
NDC Type Breakdown
24 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).
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NDC
10117-0218
Nonproprietary Name
Poloxalene
Labeler
BASF Corporation
Dosage Form
LIQUID
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