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Desipramine Hydrochloride
Desipramine Hydrochloride - 0781-1971-10 - (Desipramine Hydrochloride)
Drug Information of Desipramine Hydrochloride
| Product NDC: | 0781-1971 |
| Proprietary Name: | Desipramine Hydrochloride |
| Non Proprietary Name: | Desipramine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Desipramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desipramine Hydrochloride
| Product NDC: | 0781-1971 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072099 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880524 |
Package Information of Desipramine Hydrochloride
| Package NDC: | 0781-1971-10 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1971-10) |
NDC Information of Desipramine Hydrochloride
| NDC Code | 0781-1971-10 |
| Proprietary Name | Desipramine Hydrochloride |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1971-10) |
| Product NDC | 0781-1971 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desipramine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19880524 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | DESIPRAMINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
