Leucovorin - 25021-815-30 - (leucovorin calcium)

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Drug Information of Leucovorin

Product NDC: 25021-815
Proprietary Name: Leucovorin
Non Proprietary Name: leucovorin calcium
Active Ingredient(s): 200    mg/20mL & nbsp;   leucovorin calcium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Leucovorin

Product NDC: 25021-815
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200753
Marketing Category: ANDA
Start Marketing Date: 20120915

Package Information of Leucovorin

Package NDC: 25021-815-30
Package Description: 1 VIAL in 1 CARTON (25021-815-30) > 20 mL in 1 VIAL

NDC Information of Leucovorin

NDC Code 25021-815-30
Proprietary Name Leucovorin
Package Description 1 VIAL in 1 CARTON (25021-815-30) > 20 mL in 1 VIAL
Product NDC 25021-815
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name leucovorin calcium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20120915
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name LEUCOVORIN CALCIUM
Strength Number 200
Strength Unit mg/20mL
Pharmaceutical Classes Folate Analog [EPC],Folic Acid [Chemical/Ingredient]

Complete Information of Leucovorin


General Information