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CARBAMAZEPINE - 60505-0183-1 - (CARBAMAZEPINE)

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Drug Information of CARBAMAZEPINE

Product NDC: 60505-0183
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: 60505-0183
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075948
Marketing Category: ANDA
Start Marketing Date: 20020901

Package Information of CARBAMAZEPINE

Package NDC: 60505-0183-1
Package Description: 1000 TABLET in 1 BOTTLE (60505-0183-1)

NDC Information of CARBAMAZEPINE

NDC Code 60505-0183-1
Proprietary Name CARBAMAZEPINE
Package Description 1000 TABLET in 1 BOTTLE (60505-0183-1)
Product NDC 60505-0183
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CARBAMAZEPINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020901
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


General Information