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CARBAMAZEPINE - 76237-127-30 - (CARBAMAZEPINE)

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Drug Information of CARBAMAZEPINE

Product NDC: 76237-127
Proprietary Name: CARBAMAZEPINE
Non Proprietary Name: CARBAMAZEPINE
Active Ingredient(s): 100    mg/1 & nbsp;   CARBAMAZEPINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of CARBAMAZEPINE

Product NDC: 76237-127
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075712
Marketing Category: ANDA
Start Marketing Date: 20110901

Package Information of CARBAMAZEPINE

Package NDC: 76237-127-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-127-30) > 5 TABLET, CHEWABLE in 1 BLISTER PACK

NDC Information of CARBAMAZEPINE

NDC Code 76237-127-30
Proprietary Name CARBAMAZEPINE
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-127-30) > 5 TABLET, CHEWABLE in 1 BLISTER PACK
Product NDC 76237-127
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CARBAMAZEPINE
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20110901
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name CARBAMAZEPINE
Strength Number 100
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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