National Drug Code (NDC) Database
Vantage Specialty Ingredients, Inc.
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NDC:
80466-131
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Nonproprietary Name:
Titanium Dioxide
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.94 kg/kg
-
Substance:
TITANIUM DIOXIDE
-
Start Marketing Date:
2011-10-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Vantive US Healthcare LLC
-
NDC:
66127-100
-
Nonproprietary Name:
icodextrin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ICODEXTRIN
-
Start Marketing Date:
2006-04-21
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Vardenafil Hydrochloride Trihydrate
-
NDC:
33342-604
-
Nonproprietary Name:
Vardenafil Hydrochloride Trihydrate
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
0.5 kg/.5kg
-
Substance:
VARDENAFIL HYDROCHLORIDE
-
Start Marketing Date:
2024-05-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Vasudha Pharma Chem Limited
-
NDC:
66577-046
-
Nonproprietary Name:
Loratadine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
LORATADINE
-
Start Marketing Date:
2006-09-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Vasundhara Rasayans Limited
-
NDC:
87067-102
-
Nonproprietary Name:
MAGNESIUM HYDROXIDE
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
MAGNESIUM HYDROXIDE
-
Start Marketing Date:
2025-08-25
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Vege Labs LLC
-
NDC:
67923-109
-
Nonproprietary Name:
Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone
-
Dosage Form:
LOTION
-
Product Type:
HUMAN OTC DRUG
-
Strength:
1.5; 6.2; 7.4; 5 g/100g; g/100g; g/100g; g/100g
-
Substance:
AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE
-
Start Marketing Date:
2024-08-08
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Venator P&A Finland Oy
-
NDC:
22887-6029
-
Nonproprietary Name:
Titanium Dioxide
-
Dosage Form:
POWDER
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
0.92 kg/kg
-
Substance:
TITANIUM DIOXIDE
-
Start Marketing Date:
2011-07-25
-
End Marketing Date:
2027-03-31
-
DEA Schedule:
-
Certified Through:
0000-00-00
Veranova, L.P.
-
NDC:
50137-4245
-
Nonproprietary Name:
Dofetilide
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
DOFETILIDE
-
Start Marketing Date:
2016-06-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Vertellus LLC
-
NDC:
25441-0095
-
Nonproprietary Name:
Niacin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
25 kg/25kg
-
Substance:
NIACIN
-
Start Marketing Date:
2021-11-30
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Vifor (International) Inc.
-
NDC:
59353-652
-
Nonproprietary Name:
Iron Sucrose
-
Dosage Form:
LIQUID
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
1 kg/20L
-
Substance:
IRON SUCROSE
-
Start Marketing Date:
2009-06-24
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
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