National Drug Code (NDC) Database
Alchymars ICM SM Private Limited
-
NDC:
14998-0018
-
Nonproprietary Name:
Fosphenytoin sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FOSPHENYTOIN SODIUM
-
Start Marketing Date:
2016-11-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Alcoholera de Zapopan, S.A. de C.V.
-
NDC:
81730-002
-
Nonproprietary Name:
ALCOHOL
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 L/L
-
Substance:
ALCOHOL
-
Start Marketing Date:
2023-04-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Alcon Laboratories, Inc.
-
NDC:
70727-324
-
Nonproprietary Name:
NETARSUDIL MESYLATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
NETARSUDIL MESYLATE
-
Start Marketing Date:
2017-12-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Alfasigma SpA
-
NDC:
70799-000
-
Nonproprietary Name:
Rifaximin
-
Dosage Form:
TABLET
-
Product Type:
BULK INGREDIENT
-
Strength:
550 mg/1
-
Substance:
RIFAXIMIN
-
Start Marketing Date:
2016-07-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Alivira Animal Health Limited
-
NDC:
86055-0029
-
Nonproprietary Name:
LUFENURON
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LUFENURON
-
Start Marketing Date:
2023-05-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Alivus Life Sciences Limited
-
NDC:
66039-980
-
Nonproprietary Name:
Viloxazine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
VILOXAZINE HYDROCHLORIDE
-
Start Marketing Date:
2025-12-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Alkaloids Bioactives Private Limited
-
NDC:
85973-0001
-
Nonproprietary Name:
Colchicine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
COLCHICINE
-
Start Marketing Date:
2017-11-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
46708-942
-
Nonproprietary Name:
ACALABRUTINIB
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
ACALABRUTINIB
-
Start Marketing Date:
2025-09-11
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
50095-003
-
Nonproprietary Name:
Phenobarbital Sodium
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
PHENOBARBITAL SODIUM
-
Start Marketing Date:
2023-12-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CIV
-
Certified Through:
2026-12-31
-
NDC:
68404-1004
-
Nonproprietary Name:
Scopolamine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SCOPOLAMINE
-
Start Marketing Date:
2014-10-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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