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Carbamazepine - 0615-3505-31 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 0615-3505
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: 0615-3505
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070541
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Carbamazepine

Package NDC: 0615-3505-31
Package Description: 31 TABLET in 1 BLISTER PACK (0615-3505-31)

NDC Information of Carbamazepine

NDC Code 0615-3505-31
Proprietary Name Carbamazepine
Package Description 31 TABLET in 1 BLISTER PACK (0615-3505-31)
Product NDC 0615-3505
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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