National Drug Code (NDC) Database
NOVACYL SAS
-
NDC:
10357-788
-
Nonproprietary Name:
SALICYLIC ACID
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SALICYLIC ACID
-
Start Marketing Date:
2011-11-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Novartis Pharma Produktions GmbH
-
NDC:
66828-0324
-
Nonproprietary Name:
carbamazepine
-
Dosage Form:
TABLET, EXTENDED RELEASE
-
Product Type:
HUMAN PRESCRIPTION DRUG
-
Strength:
100 mg/1
-
Substance:
CARBAMAZEPINE
-
Start Marketing Date:
1996-03-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
NOVARTIS PHARMA SAS
-
NDC:
66447-0104
-
Nonproprietary Name:
omalizumab
-
Dosage Form:
LIQUID
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
OMALIZUMAB
-
Start Marketing Date:
2003-06-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Novo Nordisk A/S
-
NDC:
0420-9600
-
Nonproprietary Name:
semaglutide
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
2.68 mg/mL
-
Substance:
SEMAGLUTIDE
-
Start Marketing Date:
2026-04-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Novo Nordisk Production Belgium SA
-
NDC:
43835-0059
-
Nonproprietary Name:
Semaglutide
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
3.2 mg/.75mL
-
Substance:
SEMAGLUTIDE
-
Start Marketing Date:
2025-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Novo Nordisk Production Ireland Limited
-
NDC:
56125-800
-
Nonproprietary Name:
sirolimus
-
Dosage Form:
SUSPENSION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
150 g/kg
-
Substance:
SIROLIMUS
-
Start Marketing Date:
2000-08-25
-
End Marketing Date:
2028-10-01
-
DEA Schedule:
-
Certified Through:
0000-00-00
Novocol Pharmaceutical of Canada, Inc.
-
NDC:
51004-2400
-
Nonproprietary Name:
Epinephrine Injection
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 mg/mL
-
Substance:
EPINEPHRINE
-
Start Marketing Date:
2020-01-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
NR OILS
-
NDC:
81466-504
-
Nonproprietary Name:
Antifungal Drug Substance
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
ZINC UNDECYLENATE
-
Start Marketing Date:
2022-02-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
NTP RADIOISOTOPES
-
NDC:
54463-002
-
Nonproprietary Name:
FISSION IODENE
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
200 mg/20mL
-
Substance:
IODINE I-131
-
Start Marketing Date:
2013-05-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
44139-0105
-
Nonproprietary Name:
eltrombopag olamine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ELTROMBOPAG OLAMINE
-
Start Marketing Date:
2016-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
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