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Carbamazepine - 66993-407-32 - (carbamazepine)

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Drug Information of Carbamazepine

Product NDC: 66993-407
Proprietary Name: Carbamazepine
Non Proprietary Name: carbamazepine
Active Ingredient(s): 100    mg/1 & nbsp;   carbamazepine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Carbamazepine

Product NDC: 66993-407
Labeler Name: Prasco Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020712
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111215

Package Information of Carbamazepine

Package NDC: 66993-407-32
Package Description: 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (66993-407-32)

NDC Information of Carbamazepine

NDC Code 66993-407-32
Proprietary Name Carbamazepine
Package Description 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (66993-407-32)
Product NDC 66993-407
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name carbamazepine
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111215
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Prasco Laboratories
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


General Information