National Drug Code (NDC) Database
Wang Pharmaceuticals & Chemicals
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NDC:
73361-003
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Nonproprietary Name:
CHLORAMPHENICOL PALMITATE
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Dosage Form:
SALVE
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
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Substance:
CHLORAMPHENICOL PALMITATE
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Start Marketing Date:
2024-10-01
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
WanYang Hengshui Pharmaceutical Co., Ltd
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NDC:
87613-001
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Nonproprietary Name:
Anastrozole
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
ANASTROZOLE
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Start Marketing Date:
2026-04-27
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2027-12-31
Wasserburger Arzneimittelwerk GmbH
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NDC:
62287-931
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Nonproprietary Name:
Ferric Derisomaltose
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Dosage Form:
SOLUTION
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
1000 mg/10mL
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Substance:
FERRIC DERISOMALTOSE
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Start Marketing Date:
2020-10-01
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Wavelength Enterprises Ltd.
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NDC:
58175-0646
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Nonproprietary Name:
Tapinarof
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
TAPINAROF
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Start Marketing Date:
2022-03-15
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
WE Soda Alkali LLC
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NDC:
83094-105
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Nonproprietary Name:
SODIUM BICARBONATE
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Dosage Form:
CRYSTAL
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
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Substance:
SODIUM BICARBONATE
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Start Marketing Date:
2014-02-25
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Weifang Shengtai Medicine Co., Ltd.
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NDC:
40087-1001
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Nonproprietary Name:
Dextrose Monohydrate
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
DEXTROSE MONOHYDRATE
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Start Marketing Date:
2022-01-20
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Welmark International
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NDC:
11536-0019
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Nonproprietary Name:
S METHOPRENE
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Dosage Form:
LIQUID
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
METHOPRENE
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Start Marketing Date:
2009-07-25
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
Willow Birch Pharma Inc.
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NDC:
10695-114
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Nonproprietary Name:
Naltrexone HCL
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
NALTREXONE HYDROCHLORIDE
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Start Marketing Date:
2025-01-28
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
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NDC:
58175-1234
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Nonproprietary Name:
MOMETASONE FUROATE
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
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Substance:
MOMETASONE FUROATE
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Start Marketing Date:
2001-02-09
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
10695-249
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Nonproprietary Name:
Inositol
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
INOSITOL
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Start Marketing Date:
2025-11-19
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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