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Leucovorin Calcium - 51079-582-05 - (Leucovorin Calcium)

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Drug Information of Leucovorin Calcium

Product NDC: 51079-582
Proprietary Name: Leucovorin Calcium
Non Proprietary Name: Leucovorin Calcium
Active Ingredient(s): 25    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: 51079-582
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071199
Marketing Category: ANDA
Start Marketing Date: 20120824

Package Information of Leucovorin Calcium

Package NDC: 51079-582-05
Package Description: 20 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-582-05) > 1 TABLET in 1 BLISTER PACK (51079-582-01)

NDC Information of Leucovorin Calcium

NDC Code 51079-582-05
Proprietary Name Leucovorin Calcium
Package Description 20 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-582-05) > 1 TABLET in 1 BLISTER PACK (51079-582-01)
Product NDC 51079-582
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Leucovorin Calcium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120824
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name LEUCOVORIN CALCIUM
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Folate Analog [EPC],Folic Acid [Chemical/Ingredient]

Complete Information of Leucovorin Calcium


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