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Carbamazepine - 51672-4047-9 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 51672-4047
Proprietary Name: Carbamazepine
Non Proprietary Name: Carbamazepine
Active Ingredient(s): 100    mg/5mL & nbsp;   Carbamazepine
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Carbamazepine

Product NDC: 51672-4047
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076729
Marketing Category: ANDA
Start Marketing Date: 20040920

Package Information of Carbamazepine

Package NDC: 51672-4047-9
Package Description: 450 mL in 1 BOTTLE (51672-4047-9)

NDC Information of Carbamazepine

NDC Code 51672-4047-9
Proprietary Name Carbamazepine
Package Description 450 mL in 1 BOTTLE (51672-4047-9)
Product NDC 51672-4047
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20040920
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name CARBAMAZEPINE
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Complete Information of Carbamazepine


General Information