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Norpramin
Norpramin - 0068-0015-01 - (desipramine hydrochloride)
Drug Information of Norpramin
| Product NDC: | 0068-0015 |
| Proprietary Name: | Norpramin |
| Non Proprietary Name: | desipramine hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; desipramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Norpramin
| Product NDC: | 0068-0015 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA014399 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19641120 |
Package Information of Norpramin
| Package NDC: | 0068-0015-01 |
| Package Description: | 100 TABLET, SUGAR COATED in 1 BOTTLE (0068-0015-01) |
NDC Information of Norpramin
| NDC Code | 0068-0015-01 |
| Proprietary Name | Norpramin |
| Package Description | 100 TABLET, SUGAR COATED in 1 BOTTLE (0068-0015-01) |
| Product NDC | 0068-0015 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desipramine hydrochloride |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 19641120 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | DESIPRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
