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Leucovorin Calcium - 52125-453-02 - (Leucovorin Calcium)

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Drug Information of Leucovorin Calcium

Product NDC: 52125-453
Proprietary Name: Leucovorin Calcium
Non Proprietary Name: Leucovorin Calcium
Active Ingredient(s): 5    mg/1 & nbsp;   Leucovorin Calcium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Leucovorin Calcium

Product NDC: 52125-453
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071198
Marketing Category: ANDA
Start Marketing Date: 20130522

Package Information of Leucovorin Calcium

Package NDC: 52125-453-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-453-02)

NDC Information of Leucovorin Calcium

NDC Code 52125-453-02
Proprietary Name Leucovorin Calcium
Package Description 30 TABLET in 1 BLISTER PACK (52125-453-02)
Product NDC 52125-453
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Leucovorin Calcium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130522
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LEUCOVORIN CALCIUM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Folate Analog [EPC],Folic Acid [Chemical/Ingredient]

Complete Information of Leucovorin Calcium


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