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Carbamazepine - 51672-4149-1 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 51672-4149
Proprietary Name: Carbamazepine
Non Proprietary Name: Carbamazepine
Active Ingredient(s): 300    mg/1 & nbsp;   Carbamazepine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Carbamazepine

Product NDC: 51672-4149
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201106
Marketing Category: ANDA
Start Marketing Date: 20130621

Package Information of Carbamazepine

Package NDC: 51672-4149-1
Package Description: 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4149-1)

NDC Information of Carbamazepine

NDC Code 51672-4149-1
Proprietary Name Carbamazepine
Package Description 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51672-4149-1)
Product NDC 51672-4149
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130621
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name CARBAMAZEPINE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Complete Information of Carbamazepine


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