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Leucovorin Calcium - 0555-0484-01 - (Leucovorin Calcium)

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Drug Information of Leucovorin Calcium

Product NDC: 0555-0484
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: 0555-0484
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071198
Marketing Category: ANDA
Start Marketing Date: 19900630

Package Information of Leucovorin Calcium

Package NDC: 0555-0484-01
Package Description: 30 TABLET in 1 BOTTLE (0555-0484-01)

NDC Information of Leucovorin Calcium

NDC Code 0555-0484-01
Proprietary Name Leucovorin Calcium
Package Description 30 TABLET in 1 BOTTLE (0555-0484-01)
Product NDC 0555-0484
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Leucovorin Calcium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900630
Marketing Category Name ANDA
Labeler Name Barr Laboratories 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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