National Drug Code (NDC) Database
Aragen Life Sciences Limited
-
NDC:
29967-0005
-
Nonproprietary Name:
Moxifloxacin Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MOXIFLOXACIN HYDROCHLORIDE
-
Start Marketing Date:
2018-02-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Arch Chemicals Inc.
-
NDC:
11521-226
-
Nonproprietary Name:
Pyrithione Zinc
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.48 kg/kg
-
Substance:
PYRITHIONE ZINC
-
Start Marketing Date:
2009-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Arch Pharmalabs Limited
-
NDC:
22365-123
-
Nonproprietary Name:
Nitrofurantoin Monohydrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
20 kg/20kg
-
Substance:
NITROFURANTOIN MONOHYDRATE
-
Start Marketing Date:
2003-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Archimica S.p.A.
-
NDC:
55512-0026
-
Nonproprietary Name:
Cytarabine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CYTARABINE
-
Start Marketing Date:
2019-12-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Ardena US, LLC
-
NDC:
85247-0008
-
Nonproprietary Name:
Nilotinib
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
95 mg/1
-
Substance:
NILOTINIB
-
Start Marketing Date:
2025-02-04
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Arene Life Sciences Private Limited
-
NDC:
71859-007
-
Nonproprietary Name:
Phenylbutazone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PHENYLBUTAZONE
-
Start Marketing Date:
2025-12-23
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Arene life sciences ptivate limited
-
NDC:
71859-003
-
Nonproprietary Name:
phthaloyl amlodipine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
PHTHALIMIDOAMLODIPINE
-
Start Marketing Date:
2024-03-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
10094-608
-
Nonproprietary Name:
ondansetron oral film
-
Dosage Form:
FILM
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
8 mg/1
-
Substance:
ONDANSETRON
-
Start Marketing Date:
2022-02-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
10920-703
-
Nonproprietary Name:
Remifentanil Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 kg/100kg
-
Substance:
REMIFENTANIL HYDROCHLORIDE
-
Start Marketing Date:
2026-05-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2027-12-31
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