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Carbamazepine - 53808-0915-1 - (CARBAMAZEPINE)

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Drug Information of Carbamazepine

Product NDC: 53808-0915
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: 53808-0915
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075948
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Carbamazepine

Package NDC: 53808-0915-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0915-1)

NDC Information of Carbamazepine

NDC Code 53808-0915-1
Proprietary Name Carbamazepine
Package Description 30 TABLET in 1 BLISTER PACK (53808-0915-1)
Product NDC 53808-0915
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CARBAMAZEPINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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