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Carbamazepine - 68788-9812-9 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 68788-9812
Proprietary Name: Carbamazepine
Non Proprietary Name: Carbamazepine
Active Ingredient(s): 200    mg/1 & nbsp;   Carbamazepine
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Carbamazepine

Product NDC: 68788-9812
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075687
Marketing Category: ANDA
Start Marketing Date: 20120423

Package Information of Carbamazepine

Package NDC: 68788-9812-9
Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE (68788-9812-9)

NDC Information of Carbamazepine

NDC Code 68788-9812-9
Proprietary Name Carbamazepine
Package Description 90 TABLET, CHEWABLE in 1 BOTTLE (68788-9812-9)
Product NDC 68788-9812
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20120423
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
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


General Information