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Levocarnitine - 55390-136-05 - (Levocarnitine)

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Drug Information of Levocarnitine

Product NDC: 55390-136
Proprietary Name: Levocarnitine
Non Proprietary Name: Levocarnitine
Active Ingredient(s): 1    g/5mL & nbsp;   Levocarnitine
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levocarnitine

Product NDC: 55390-136
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075567
Marketing Category: ANDA
Start Marketing Date: 20010423

Package Information of Levocarnitine

Package NDC: 55390-136-05
Package Description: 10 VIAL in 1 BOX (55390-136-05) > 5 mL in 1 VIAL

NDC Information of Levocarnitine

NDC Code 55390-136-05
Proprietary Name Levocarnitine
Package Description 10 VIAL in 1 BOX (55390-136-05) > 5 mL in 1 VIAL
Product NDC 55390-136
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levocarnitine
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20010423
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name LEVOCARNITINE
Strength Number 1
Strength Unit g/5mL
Pharmaceutical Classes Carnitine [Chemical/Ingredient],Carnitine Analog [EPC]

Complete Information of Levocarnitine


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