National Drug Code (NDC) Database
Celgene Chemicals Sarl
-
NDC:
82991-402
-
Nonproprietary Name:
LENALIDOMIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LENALIDOMIDE
-
Start Marketing Date:
2008-08-28
-
End Marketing Date:
2027-01-02
-
DEA Schedule:
-
Certified Through:
0000-00-00
Celgene International Sarl
-
NDC:
43593-803
-
Nonproprietary Name:
ozanimod hydrochloride
-
Dosage Form:
CAPSULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.23 mg/1
-
Substance:
OZANIMOD HYDROCHLORIDE
-
Start Marketing Date:
2020-03-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Celltrion Branchburg, LLC
-
NDC:
73424-0561
-
Nonproprietary Name:
Cetuximab
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CETUXIMAB
-
Start Marketing Date:
2004-02-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
CELLTRION, Inc
-
NDC:
32228-020
-
Nonproprietary Name:
bevacizumab-adcd
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 mg/4mL
-
Substance:
BEVACIZUMAB-ADCD
-
Start Marketing Date:
2023-04-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
CELLTRION, Inc.
-
NDC:
32228-022
-
Nonproprietary Name:
infliximab-dyyb
-
Dosage Form:
INJECTION
-
Product Type:
BULK INGREDIENT
-
Strength:
9 kg/9kg
-
Substance:
INFLIXIMAB-DYYB
-
Start Marketing Date:
2024-03-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Centaur Pharmaceuticals Private Limited
-
NDC:
64330-670
-
Nonproprietary Name:
Pyridostigmine Bromide
-
Dosage Form:
GRANULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
30 mg/1
-
Substance:
PYRIDOSTIGMINE BROMIDE
-
Start Marketing Date:
2019-01-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Central Glass Co.,Ltd.
-
NDC:
54122-4486
-
Nonproprietary Name:
SEVOFLURANE
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
500 L/500L
-
Substance:
SEVOFLURANE
-
Start Marketing Date:
1995-07-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Central Indiana Ethanol, LLC
-
NDC:
72438-010
-
Nonproprietary Name:
Alcohol
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
95 L/100L
-
Substance:
ALCOHOL
-
Start Marketing Date:
2022-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
84577-750
-
Nonproprietary Name:
Gedatolisib
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GEDATOLISIB
-
Start Marketing Date:
2026-01-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
59572-816
-
Nonproprietary Name:
ozanimod hydrochloride
-
Dosage Form:
CAPSULE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.92 mg/1
-
Substance:
OZANIMOD HYDROCHLORIDE
-
Start Marketing Date:
2020-03-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Create a New Buying Request
Fields marked with * are mandatory.