Product NDC: | 13668-268 |
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) |
Product NDC: | 13668-268 |
Labeler Name: | Torrent Pharmaceuticals Limited |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077272 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091023 |
Package NDC: | 13668-268-31 |
Package Description: | 2500 TABLET in 1 BOTTLE (13668-268-31) |
NDC Code | 13668-268-31 |
Proprietary Name | CARBAMAZEPINE |
Package Description | 2500 TABLET in 1 BOTTLE (13668-268-31) |
Product NDC | 13668-268 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CARBAMAZEPINE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20091023 |
Marketing Category Name | ANDA |
Labeler Name | Torrent Pharmaceuticals Limited |
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] |