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imipramine hydrochloride
imipramine hydrochloride - 63629-1510-2 - (imipramine hydrochloride)
Drug Information of imipramine hydrochloride
| Product NDC: | 63629-1510 |
| Proprietary Name: | imipramine hydrochloride |
| Non Proprietary Name: | imipramine hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; imipramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of imipramine hydrochloride
| Product NDC: | 63629-1510 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA081050 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900605 |
Package Information of imipramine hydrochloride
| Package NDC: | 63629-1510-2 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (63629-1510-2) |
NDC Information of imipramine hydrochloride
| NDC Code | 63629-1510-2 |
| Proprietary Name | imipramine hydrochloride |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (63629-1510-2) |
| Product NDC | 63629-1510 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | imipramine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19900605 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | IMIPRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
