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Carbamazepine - 54868-6074-0 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 54868-6074
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: 54868-6074
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020234
Marketing Category: NDA
Start Marketing Date: 20091016

Package Information of Carbamazepine

Package NDC: 54868-6074-0
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-6074-0)

NDC Information of Carbamazepine

NDC Code 54868-6074-0
Proprietary Name Carbamazepine
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (54868-6074-0)
Product NDC 54868-6074
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20091016
Marketing Category Name NDA
Labeler Name Physicians Total Care, 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


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