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Carbamazepine - 60505-2806-0 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 60505-2806
Proprietary Name: Carbamazepine
Non Proprietary Name: Carbamazepine
Active Ingredient(s): 200    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: 60505-2806
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078986
Marketing Category: ANDA
Start Marketing Date: 20120323

Package Information of Carbamazepine

Package NDC: 60505-2806-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-2806-0) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Carbamazepine

NDC Code 60505-2806-0
Proprietary Name Carbamazepine
Package Description 10 BLISTER PACK in 1 CARTON (60505-2806-0) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 60505-2806
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120323
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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