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LEVOCARNITINE - 64980-130-09 - (LEVOCARNITINE)

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Drug Information of LEVOCARNITINE

Product NDC: 64980-130
Proprietary Name: LEVOCARNITINE
Non Proprietary Name: LEVOCARNITINE
Active Ingredient(s): 330    mg/1 & nbsp;   LEVOCARNITINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LEVOCARNITINE

Product NDC: 64980-130
Labeler Name: Rising Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076858
Marketing Category: ANDA
Start Marketing Date: 20040920

Package Information of LEVOCARNITINE

Package NDC: 64980-130-09
Package Description: 9 BLISTER PACK in 1 BOX (64980-130-09) > 10 TABLET in 1 BLISTER PACK

NDC Information of LEVOCARNITINE

NDC Code 64980-130-09
Proprietary Name LEVOCARNITINE
Package Description 9 BLISTER PACK in 1 BOX (64980-130-09) > 10 TABLET in 1 BLISTER PACK
Product NDC 64980-130
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LEVOCARNITINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040920
Marketing Category Name ANDA
Labeler Name Rising Pharmaceuticals, Inc.
Substance Name LEVOCARNITINE
Strength Number 330
Strength Unit mg/1
Pharmaceutical Classes Carnitine [Chemical/Ingredient],Carnitine Analog [EPC]

Complete Information of LEVOCARNITINE


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