Home
>
National Drug Code (NDC)
>
Quinapril Hydrochloride
Quinapril Hydrochloride - 59762-5019-1 - (QUINAPRIL HYDROCHLORIDE)
Drug Information of Quinapril Hydrochloride
| Product NDC: | 59762-5019 |
| Proprietary Name: | Quinapril Hydrochloride |
| Non Proprietary Name: | QUINAPRIL HYDROCHLORIDE |
| Active Ingredient(s): | 5 mg/1 & nbsp; QUINAPRIL HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Quinapril Hydrochloride
| Product NDC: | 59762-5019 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019885 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19911119 |
Package Information of Quinapril Hydrochloride
| Package NDC: | 59762-5019-1 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (59762-5019-1) |
NDC Information of Quinapril Hydrochloride
| NDC Code | 59762-5019-1 |
| Proprietary Name | Quinapril Hydrochloride |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (59762-5019-1) |
| Product NDC | 59762-5019 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | QUINAPRIL HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19911119 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | QUINAPRIL HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
