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Carbamazepine - 43063-328-12 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 43063-328
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: 43063-328
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074649
Marketing Category: ANDA
Start Marketing Date: 19961003

Package Information of Carbamazepine

Package NDC: 43063-328-12
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC (43063-328-12)

NDC Information of Carbamazepine

NDC Code 43063-328-12
Proprietary Name Carbamazepine
Package Description 12 TABLET in 1 BOTTLE, PLASTIC (43063-328-12)
Product NDC 43063-328
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 PD-Rx Pharmaceuticals, 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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