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Moexipril Hydrochloride
Moexipril Hydrochloride - 0093-5150-01 - (Moexipril Hydrochloride)
Drug Information of Moexipril Hydrochloride
| Product NDC: | 0093-5150 |
| Proprietary Name: | Moexipril Hydrochloride |
| Non Proprietary Name: | Moexipril Hydrochloride |
| Active Ingredient(s): | 15 mg/1 & nbsp; Moexipril Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Moexipril Hydrochloride
| Product NDC: | 0093-5150 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076204 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030508 |
Package Information of Moexipril Hydrochloride
| Package NDC: | 0093-5150-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5150-01) |
NDC Information of Moexipril Hydrochloride
| NDC Code | 0093-5150-01 |
| Proprietary Name | Moexipril Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5150-01) |
| Product NDC | 0093-5150 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Moexipril Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030508 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | MOEXIPRIL HYDROCHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
