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Carbamazepine - 63739-045-01 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 63739-045
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: 63739-045
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070541
Marketing Category: ANDA
Start Marketing Date: 20040901

Package Information of Carbamazepine

Package NDC: 63739-045-01
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-045-01) > 30 TABLET in 1 BLISTER PACK

NDC Information of Carbamazepine

NDC Code 63739-045-01
Proprietary Name Carbamazepine
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-045-01) > 30 TABLET in 1 BLISTER PACK
Product NDC 63739-045
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040901
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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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