Tegretol - 0078-0509-05 - (carbamazepine)

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Drug Information of Tegretol

Product NDC: 0078-0509
Proprietary Name: Tegretol
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 Tegretol

Product NDC: 0078-0509
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016608
Marketing Category: NDA
Start Marketing Date: 19680311

Package Information of Tegretol

Package NDC: 0078-0509-05
Package Description: 100 TABLET in 1 BOTTLE (0078-0509-05)

NDC Information of Tegretol

NDC Code 0078-0509-05
Proprietary Name Tegretol
Package Description 100 TABLET in 1 BOTTLE (0078-0509-05)
Product NDC 0078-0509
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name carbamazepine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19680311
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
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 Tegretol


General Information