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MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE - 54868-3443-1 - (moexipril hydrochloride and hydrochlorothiazide)
Drug Information of MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
| Product NDC: | 54868-3443 |
| Proprietary Name: | MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE |
| Non Proprietary Name: | moexipril hydrochloride and hydrochlorothiazide |
| Active Ingredient(s): | 25; 15 mg/1; mg/1 & nbsp; moexipril hydrochloride and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
| Product NDC: | 54868-3443 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076980 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070516 |
Package Information of MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
| Package NDC: | 54868-3443-1 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-3443-1) |
NDC Information of MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
| NDC Code | 54868-3443-1 |
| Proprietary Name | MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-3443-1) |
| Product NDC | 54868-3443 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | moexipril hydrochloride and hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070516 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE |
| Strength Number | 25; 15 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
