National Drug Code (NDC) Database
Sumar Biotech LLP
-
NDC:
85705-001
-
Nonproprietary Name:
SIROLIMUS
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
SIROLIMUS
-
Start Marketing Date:
2025-06-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sumitomo Chemical Co., Ltd.
-
NDC:
68259-1318
-
Nonproprietary Name:
Sofpironium bromide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SOFPIRONIUM BROMIDE
-
Start Marketing Date:
2024-12-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sumitomo Chemical Company, Limited
-
NDC:
68259-1317
-
Nonproprietary Name:
lurasidone hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LURASIDONE HYDROCHLORIDE
-
Start Marketing Date:
2024-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SUMITOMO OSAKA CEMENT CO. LTD.
-
NDC:
69253-008
-
Nonproprietary Name:
ZINC OXIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2025-10-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Sumitomo Pharma Co., Ltd.
-
NDC:
38217-0040
-
Nonproprietary Name:
Zonisamide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ZONISAMIDE
-
Start Marketing Date:
2019-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SUN PHARMACEUTICAL IND LTD, MUMBAI
-
NDC:
62756-171
-
Nonproprietary Name:
Dapagliflozin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
DAPAGLIFLOZIN
-
Start Marketing Date:
2017-02-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
SUN PHARMACEUTICAL INDUSTRIES, INC.
-
NDC:
70095-218
-
Nonproprietary Name:
Methylnaltrexone Bromide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
METHYLNALTREXONE BROMIDE
-
Start Marketing Date:
2026-06-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
SUNJIN BEAUTY SCIENCE CO., LTD.
-
NDC:
71028-9111
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2019-07-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
SUNLIT FLUO & CHEMICAL CO., L TD. CHUNG-LI FACTORY
-
NDC:
62505-001
-
Nonproprietary Name:
Natrium Fluoride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SODIUM FLUORIDE
-
Start Marketing Date:
2011-01-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
54907-0141
-
Nonproprietary Name:
Cariprazine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
CARIPRAZINE HYDROCHLORIDE
-
Start Marketing Date:
2026-06-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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