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Carbamazepine - 51079-385-19 - (Carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 51079-385
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: 51079-385
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070541
Marketing Category: ANDA
Start Marketing Date: 20111028

Package Information of Carbamazepine

Package NDC: 51079-385-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-385-19) > 17 TABLET in 1 BLISTER PACK (51079-385-17)

NDC Information of Carbamazepine

NDC Code 51079-385-19
Proprietary Name Carbamazepine
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-385-19) > 17 TABLET in 1 BLISTER PACK (51079-385-17)
Product NDC 51079-385
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbamazepine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111028
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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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