National Drug Code (NDC) Database
Hong Kong Xile International Trading Limited
-
NDC:
85209-003
-
Nonproprietary Name:
Maropitant Citrate
-
Dosage Form:
TABLET
-
Product Type:
BULK INGREDIENT
-
Strength:
60 mg/60mg
-
Substance:
MAROPITANT CITRATE
-
Start Marketing Date:
2025-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
HONOUR LAB LIMITED
-
NDC:
82708-0017
-
Nonproprietary Name:
Ticagrelor
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
TICAGRELOR
-
Start Marketing Date:
2015-09-03
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Horizon Sopyrwa Ltd
-
NDC:
72273-364
-
Nonproprietary Name:
pyrethrum extract
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 kg/200kg
-
Substance:
PYRETHRUM EXTRACT
-
Start Marketing Date:
2001-01-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
HORSTER BIOTEK PVT LTD.
-
NDC:
85568-006
-
Nonproprietary Name:
TADALAFIL
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
100 g/100g
-
Substance:
TADALAFIL
-
Start Marketing Date:
2025-04-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
HORSTER LIFE SCIENCE PVT LTD
-
NDC:
85617-003
-
Nonproprietary Name:
Ivermectin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
IVERMECTIN
-
Start Marketing Date:
2025-05-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Hospira Zagreb d.o.o.
-
NDC:
71861-0234
-
Nonproprietary Name:
anakinra
-
Dosage Form:
INJECTION, SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
100 mg/.67mL
-
Substance:
ANAKINRA
-
Start Marketing Date:
2020-10-28
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
HOVIONE FARMACIENCIA S.A.
-
NDC:
50909-1906
-
Nonproprietary Name:
Solid Dispersion of BMS-986165-01
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.15 kg/kg
-
Substance:
DEUCRAVACITINIB
-
Start Marketing Date:
2022-07-05
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
HOVIONE FARMACIÊNCIA, S.A.
-
NDC:
50909-1704
-
Nonproprietary Name:
Plazomicin sulfate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
PLAZOMICIN SULFATE
-
Start Marketing Date:
2018-06-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
0662-4887
-
Nonproprietary Name:
water
-
Dosage Form:
INJECTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 mL/mL
-
Substance:
WATER
-
Start Marketing Date:
2019-12-18
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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