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Quinapril Hydrochloride
Quinapril Hydrochloride - 43063-358-90 - (quinapril hydrochloride)
Drug Information of Quinapril Hydrochloride
| Product NDC: | 43063-358 |
| Proprietary Name: | Quinapril Hydrochloride |
| Non Proprietary Name: | quinapril hydrochloride |
| Active Ingredient(s): | 10 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: | 43063-358 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| 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: | 43063-358-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-358-90) |
NDC Information of Quinapril Hydrochloride
| NDC Code | 43063-358-90 |
| Proprietary Name | Quinapril Hydrochloride |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-358-90) |
| Product NDC | 43063-358 |
| 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 | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | QUINAPRIL HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
