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Carbamazepine - 50436-3415-3 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 50436-3415
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: 50436-3415
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074649
Marketing Category: ANDA
Start Marketing Date: 19961003

Package Information of Carbamazepine

Package NDC: 50436-3415-3
Package Description: 90 TABLET in 1 BOTTLE (50436-3415-3)

NDC Information of Carbamazepine

NDC Code 50436-3415-3
Proprietary Name Carbamazepine
Package Description 90 TABLET in 1 BOTTLE (50436-3415-3)
Product NDC 50436-3415
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19961003
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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