National Drug Code (NDC) Database
Corden Pharma Bergamo SpA
-
NDC:
49964-0102
-
Nonproprietary Name:
Trofinetide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TROFINETIDE
-
Start Marketing Date:
2022-12-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Corden Pharma Boulder, Inc.
-
NDC:
42533-114
-
Nonproprietary Name:
TROMETHAMINE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
23 kg/23kg
-
Substance:
TROMETHAMINE
-
Start Marketing Date:
2009-11-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
CORDEN PHARMA CHENOVE
-
NDC:
61121-0005
-
Nonproprietary Name:
DURLOBACTAM SODIUM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DURLOBACTAM SODIUM
-
Start Marketing Date:
2023-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Corden Pharma Colorado, Inc.
-
NDC:
12869-803
-
Nonproprietary Name:
Ganciclovir
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GANCICLOVIR
-
Start Marketing Date:
2003-04-22
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Corden Pharma Fribourg SA
-
NDC:
83300-231
-
Nonproprietary Name:
diroximel fumarate
-
Dosage Form:
CAPSULE, DELAYED RELEASE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
231 mg/1
-
Substance:
DIROXIMEL FUMARATE
-
Start Marketing Date:
2023-12-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Corden Pharma GmbH
-
NDC:
43265-7779
-
Nonproprietary Name:
Resmetirom
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 mg/1
-
Substance:
RESMETIROM
-
Start Marketing Date:
2025-02-06
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
CoreRx, Inc.
-
NDC:
51767-228
-
Nonproprietary Name:
AMPHETAMINE SULFATE
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
10 mg/1
-
Substance:
AMPHETAMINE SULFATE
-
Start Marketing Date:
2020-01-15
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
CII
-
Certified Through:
2026-12-31
Cosmo SpA
-
NDC:
68743-882
-
Nonproprietary Name:
NALOXEGOL OXALATE
-
Dosage Form:
TABLET, FILM COATED
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
25 mg/1
-
Substance:
NALOXEGOL OXALATE
-
Start Marketing Date:
2023-03-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
65373-5390
-
Nonproprietary Name:
Pafolacianine sodium
-
Dosage Form:
INJECTION, POWDER, FOR SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 kg/kg
-
Substance:
PAFOLACIANINE SODIUM
-
Start Marketing Date:
2022-09-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
51604-1183
-
Nonproprietary Name:
LEVOMILNACIPRAN HYDROCHLORIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LEVOMILNACIPRAN HYDROCHLORIDE
-
Start Marketing Date:
2018-11-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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