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Tegretol
Tegretol - 0078-0492-35 - (carbamazepine)
Drug Information of Tegretol
| Product NDC: | 0078-0492 |
| Proprietary Name: | Tegretol |
| 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 Tegretol
| Product NDC: | 0078-0492 |
| Labeler Name: | Novartis Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018281 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19811214 |
Package Information of Tegretol
| Package NDC: | 0078-0492-35 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0492-35) > 1 TABLET, CHEWABLE in 1 BLISTER PACK (0078-0492-61) |
NDC Information of Tegretol
| NDC Code | 0078-0492-35 |
| Proprietary Name | Tegretol |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0492-35) > 1 TABLET, CHEWABLE in 1 BLISTER PACK (0078-0492-61) |
| Product NDC | 0078-0492 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | carbamazepine |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 19811214 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| 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] |
