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Carbamazepine - 0781-5088-01 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 0781-5088
Proprietary Name: Carbamazepine
Non Proprietary Name: Carbamazepine
Active Ingredient(s): 400    mg/1 & nbsp;   Carbamazepine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Carbamazepine

Product NDC: 0781-5088
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020234
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19960325

Package Information of Carbamazepine

Package NDC: 0781-5088-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5088-01)

NDC Information of Carbamazepine

NDC Code 0781-5088-01
Proprietary Name Carbamazepine
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5088-01)
Product NDC 0781-5088
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19960325
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Sandoz Inc
Substance Name CARBAMAZEPINE
Strength Number 400
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


General Information