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Carbamazepine - 49349-677-24 - (CARBAMAZEPINE)

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Drug Information of Carbamazepine

Product NDC: 49349-677
Proprietary Name: Carbamazepine
Non Proprietary Name: CARBAMAZEPINE
Active Ingredient(s): 200    mg/1 & nbsp;   CARBAMAZEPINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carbamazepine

Product NDC: 49349-677
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070541
Marketing Category: ANDA
Start Marketing Date: 20120904

Package Information of Carbamazepine

Package NDC: 49349-677-24
Package Description: 200 TABLET in 1 BLISTER PACK (49349-677-24)

NDC Information of Carbamazepine

NDC Code 49349-677-24
Proprietary Name Carbamazepine
Package Description 200 TABLET in 1 BLISTER PACK (49349-677-24)
Product NDC 49349-677
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CARBAMAZEPINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120904
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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


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