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Carbamazepine - 55154-3026-0 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 55154-3026
Proprietary Name: Carbamazepine
Non Proprietary Name: Carbamazepine
Active Ingredient(s): 200    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: 55154-3026
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078115
Marketing Category: ANDA
Start Marketing Date: 20090331

Package Information of Carbamazepine

Package NDC: 55154-3026-0
Package Description: 10 POUCH in 1 BAG (55154-3026-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH

NDC Information of Carbamazepine

NDC Code 55154-3026-0
Proprietary Name Carbamazepine
Package Description 10 POUCH in 1 BAG (55154-3026-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH
Product NDC 55154-3026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090331
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CARBAMAZEPINE
Strength Number 200
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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