National Drug Code (NDC) Database
Excella GmbH Co. KG
-
NDC:
46014-1054
-
Nonproprietary Name:
Ganciclovir Sodium
-
Dosage Form:
INJECTION
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
GANCICLOVIR SODIUM
-
Start Marketing Date:
2005-06-16
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
EZUF NL B.V
-
NDC:
15613-512
-
Nonproprietary Name:
Zinc oxide dispersion
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
21 kg/35kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2023-07-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
EZUF NL B.V.
-
NDC:
15613-610
-
Nonproprietary Name:
Zinc oxide
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
12.96 kg/14kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2015-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
F. Hoffmann-La Roche AG
-
NDC:
12806-0917
-
Nonproprietary Name:
atezolizumab
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 L/L
-
Substance:
ATEZOLIZUMAB
-
Start Marketing Date:
2016-05-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
F. Hoffmann-La Roche Ltd
-
NDC:
12806-8770
-
Nonproprietary Name:
BALOXAVIR MARBOXIL
-
Dosage Form:
TABLET
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
80 mg/1
-
Substance:
BALOXAVIR MARBOXIL
-
Start Marketing Date:
2021-03-26
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
F. Hunziker + Co AG
-
NDC:
85353-003
-
Nonproprietary Name:
ORNITHOGALUM UMBELLATUM, PRUNUS CERASIFERA, CLEMATIS VITALBA, HELIANTHEMUM NUMMULARIUM, IMPATIENS GLANDULIFERA
-
Dosage Form:
PASTILLE
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
5; 5; 5; 5; 5 1; 1; 1; 1; 1
-
Substance:
CLEMATIS VITALBA FLOWER; HELIANTHEMUM NUMMULARIUM FLOWER; IMPATIENS GLANDULIFERA FLOWER; ORNITHOGALUM UMBELLATUM FLOWERING TOP; PRUNUS CERASIFERA FLOWER
-
Start Marketing Date:
2025-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
F.I.S. - Fabbrica Italiana Sintetici S.p.A.
-
NDC:
48087-0172
-
Nonproprietary Name:
LENACAPAVIR SODIUM
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LENACAPAVIR SODIUM
-
Start Marketing Date:
2026-05-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
F.I.S. Fabbrica Italiana Sintetici S.P.A.
-
NDC:
52133-0045
-
Nonproprietary Name:
Fosaprepitant Dimeglumine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
FOSAPREPITANT DIMEGLUMINE
-
Start Marketing Date:
2010-11-12
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
60155-010
-
Nonproprietary Name:
Sacubitril Valsartan Trisodium Hemi Pentahydrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
SACUBITRIL VALSARTAN
-
Start Marketing Date:
2026-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
48087-0144
-
Nonproprietary Name:
CLOMIPHENE CITRATE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
CLOMIPHENE CITRATE
-
Start Marketing Date:
2019-03-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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