Carnitor - 54482-144-07 - (levocarnitine)

Alphabetical Index


Drug Information of Carnitor

Product NDC: 54482-144
Proprietary Name: Carnitor
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 Carnitor

Product NDC: 54482-144
Labeler Name: Sigma-Tau Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018948
Marketing Category: NDA
Start Marketing Date: 19851227

Package Information of Carnitor

Package NDC: 54482-144-07
Package Description: 10 BLISTER PACK in 1 CARTON (54482-144-07) > 9 TABLET in 1 BLISTER PACK

NDC Information of Carnitor

NDC Code 54482-144-07
Proprietary Name Carnitor
Package Description 10 BLISTER PACK in 1 CARTON (54482-144-07) > 9 TABLET in 1 BLISTER PACK
Product NDC 54482-144
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levocarnitine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19851227
Marketing Category Name NDA
Labeler Name Sigma-Tau Pharmaceuticals, Inc.
Substance Name LEVOCARNITINE
Strength Number 330
Strength Unit mg/1
Pharmaceutical Classes Carnitine [Chemical/Ingredient],Carnitine Analog [EPC]

Complete Information of Carnitor


General Information