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CARBAMAZEPINE - 55154-3975-9 - (CARBAMAZEPINE)

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Drug Information of CARBAMAZEPINE

Product NDC: 55154-3975
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: 55154-3975
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077272
Marketing Category: ANDA
Start Marketing Date: 20091023

Package Information of CARBAMAZEPINE

Package NDC: 55154-3975-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-3975-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of CARBAMAZEPINE

NDC Code 55154-3975-9
Proprietary Name CARBAMAZEPINE
Package Description 6 BLISTER PACK in 1 CARTON (55154-3975-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-3975
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CARBAMAZEPINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091023
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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