National Drug Code (NDC) Database
Millicent US, Inc.
-
NDC:
72495-600
-
Nonproprietary Name:
norethindrone acetate/ethinyl estradiol
-
Dosage Form:
KIT
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
-
Substance:
-
Start Marketing Date:
2025-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Minakem Beuvry Production
-
NDC:
70219-0004
-
Nonproprietary Name:
Azaperone
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AZAPERONE
-
Start Marketing Date:
2025-10-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Minakem Dunkerque Production
-
NDC:
49927-0006
-
Nonproprietary Name:
Esomeprazole mgdi micro
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ESOMEPRAZOLE MAGNESIUM DIHYDRATE
-
Start Marketing Date:
2015-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Minakem High Potent SA
-
NDC:
69910-0004
-
Nonproprietary Name:
Vinorelbine Tartrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 g/g
-
Substance:
VINORELBINE TARTRATE
-
Start Marketing Date:
2015-06-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
MINSHENG GROUP SHAOXING PHARMACEUTICAL CO,. LTD.
-
NDC:
13371-488
-
Nonproprietary Name:
ATROPINE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ATROPINE
-
Start Marketing Date:
2011-05-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
MINSHENG GROUP SHAOXING PHARMACEUTICAL CO., LTD.
-
NDC:
13371-789
-
Nonproprietary Name:
MORANTEL TARTRATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MORANTEL TARTRATE
-
Start Marketing Date:
2017-11-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
68995-000
-
Nonproprietary Name:
DIHYDROERGOTAMINE MESYLATE
-
Dosage Form:
SPRAY
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
4 mg/mL
-
Substance:
DIHYDROERGOTAMINE MESYLATE
-
Start Marketing Date:
2021-09-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
22607-311
-
Nonproprietary Name:
Sulbactam for injection
-
Dosage Form:
INJECTION, POWDER, FOR SOLUTION
-
Product Type:
HUMAN PRESCRIPTION DRUG
-
Strength:
1 g/5mL
-
Substance:
SULBACTAM SODIUM
-
Start Marketing Date:
2023-06-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Miyoshi America Inc.
-
NDC:
76002-0130
-
Nonproprietary Name:
Titanium Dioxide
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.7025 kg/kg
-
Substance:
TITANIUM DIOXIDE
-
Start Marketing Date:
2018-07-20
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
65376-3630
-
Nonproprietary Name:
Calcium Carbonate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CALCIUM CARBONATE
-
Start Marketing Date:
2004-10-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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