National Drug Code (NDC) Database
Teva Czech Industries s.r.o.
-
NDC:
47848-062
-
Nonproprietary Name:
ZAVEGEPANT HCL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ZAVEGEPANT HYDROCHLORIDE
-
Start Marketing Date:
2023-12-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Teva Pharmaceuticals USA, Inc.
-
NDC:
50111-561
-
Nonproprietary Name:
Trazodone Hydrochloride
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 mg/1
-
Substance:
TRAZODONE HYDROCHLORIDE
-
Start Marketing Date:
2025-06-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Teva Pharmaceuticals, Inc.
-
NDC:
0480-9242
-
Nonproprietary Name:
Propylthiouracil
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
50 mg/1
-
Substance:
PROPYLTHIOURACIL
-
Start Marketing Date:
2023-10-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Thaeta Scientific LLC
-
NDC:
87155-110
-
Nonproprietary Name:
Beta Nicotinamide Adenine Dinucleotide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
NICOTINAMIDE ADENINE DINUCLEOTIDE
-
Start Marketing Date:
2025-11-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Thatcher Company
-
NDC:
30032-551
-
Nonproprietary Name:
Povidone-Iodine
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 kg/kg
-
Substance:
POVIDONE-IODINE
-
Start Marketing Date:
2013-03-29
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
66008-1650
-
Nonproprietary Name:
ASPIRIN
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.9 kg/kg
-
Substance:
ASPIRIN
-
Start Marketing Date:
2005-09-09
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
The HallStar Company
-
NDC:
67278-2100
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
19.24 kg/19.24kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2021-07-02
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
The Procter & Gamble Manufacturing Company
-
NDC:
69423-110
-
Nonproprietary Name:
Selenium Sulfide Slurry Pre-Mix
-
Dosage Form:
SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
29.41 kg/100kg
-
Substance:
SELENIUM SULFIDE
-
Start Marketing Date:
2010-08-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
The United Laboratories (Inner Mongolia) Co., Ltd.
-
NDC:
52115-000
-
Nonproprietary Name:
6-AMINOPENICILLANIC ACID
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
6-AMINOPENICILLANIC ACID
-
Start Marketing Date:
2013-06-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
51846-1059
-
Nonproprietary Name:
Trilaciclib Hemi-Citrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TRILACICLIB
-
Start Marketing Date:
2024-10-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Create a New Buying Request
Fields marked with * are mandatory.