National Drug Code (NDC) Database
K. Patel Phyto Extractions Private Limited
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NDC:
73276-008
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Nonproprietary Name:
Coffee bean dry extract 40% (Green Coffee)
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Dosage Form:
POWDER
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Product Type:
BULK INGREDIENT
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Strength:
25 kg/25kg
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Substance:
ARABICA COFFEE BEAN
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Start Marketing Date:
2025-06-25
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
60897-170
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Nonproprietary Name:
EPA965EE
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Dosage Form:
OIL
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Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
ICOSAPENT ETHYL
-
Start Marketing Date:
2015-11-19
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End Marketing Date:
0000-00-00
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DEA Schedule:
-
Certified Through:
2026-12-31
K.S.PEARL CO., LTD.
-
NDC:
70979-504
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Nonproprietary Name:
Zinc Oxide
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Dosage Form:
POWDER
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Product Type:
DRUG FOR FURTHER PROCESSING
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Strength:
19.2 kg/20kg
-
Substance:
ZINC OXIDE
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Start Marketing Date:
2024-03-04
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kaiping Genuine Biochemical Pharmaceutical Co., Ltd.
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NDC:
85368-001
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Nonproprietary Name:
Glutathione (L-) Reduced
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
GLUTATHIONE
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Start Marketing Date:
2025-04-07
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
KAKEN Pharmaceutical Co., LTD
-
NDC:
51265-541
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Nonproprietary Name:
EFINACONAZOLE
-
Dosage Form:
SOLUTION
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Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 mg/mL
-
Substance:
EFINACONAZOLE
-
Start Marketing Date:
2014-06-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Kaken Pharmaceutical Co., Ltd.
-
NDC:
51265-363
-
Nonproprietary Name:
Butenafine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
BUTENAFINE HYDROCHLORIDE
-
Start Marketing Date:
1996-12-31
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
KALCHEM INTERNATIONAL INC.
-
NDC:
60592-918
-
Nonproprietary Name:
MINOCYCLINE
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
MINOCYCLINE HYDROCHLORIDE
-
Start Marketing Date:
2023-10-16
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End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
KALINTIS HEALTHCARE PRIVATE LIMITED
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NDC:
72166-026
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Nonproprietary Name:
FERRIC CARBOXYMALTOSE
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Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
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Strength:
1 kg/kg
-
Substance:
FERRIC CARBOXYMALTOSE
-
Start Marketing Date:
2025-02-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
60592-998
-
Nonproprietary Name:
URSODIOL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
URSODIOL
-
Start Marketing Date:
2019-12-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
84678-001
-
Nonproprietary Name:
EFINACONAZOLE
-
Dosage Form:
POWDER, FOR SOLUTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
EFINACONAZOLE
-
Start Marketing Date:
2024-07-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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