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Surmontil
Surmontil - 51285-539-02 - (Trimipramine Maleate)
Drug Information of Surmontil
| Product NDC: | 51285-539 |
| Proprietary Name: | Surmontil |
| Non Proprietary Name: | Trimipramine Maleate |
| Active Ingredient(s): | 50 mg/1 & nbsp; Trimipramine Maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Surmontil
| Product NDC: | 51285-539 |
| Labeler Name: | Duramed Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016792 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19790612 |
Package Information of Surmontil
| Package NDC: | 51285-539-02 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (51285-539-02) |
NDC Information of Surmontil
| NDC Code | 51285-539-02 |
| Proprietary Name | Surmontil |
| Package Description | 100 CAPSULE in 1 BOTTLE (51285-539-02) |
| Product NDC | 51285-539 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Trimipramine Maleate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19790612 |
| Marketing Category Name | NDA |
| Labeler Name | Duramed Pharmaceuticals Inc |
| Substance Name | TRIMIPRAMINE MALEATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
