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LISINOPRIL AND HYDROCHLOROTHIAZIDE
LISINOPRIL AND HYDROCHLOROTHIAZIDE - 68084-519-21 - (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
Drug Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE
| Product NDC: | 68084-519 |
| Proprietary Name: | LISINOPRIL AND HYDROCHLOROTHIAZIDE |
| Non Proprietary Name: | LISINOPRIL AND HYDROCHLOROTHIAZIDE |
| Active Ingredient(s): | 25; 20 mg/1; mg/1 & nbsp; LISINOPRIL AND HYDROCHLOROTHIAZIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE
| Product NDC: | 68084-519 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077912 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130612 |
Package Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE
| Package NDC: | 68084-519-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-519-21) > 10 TABLET in 1 BLISTER PACK (68084-519-11) |
NDC Information of LISINOPRIL AND HYDROCHLOROTHIAZIDE
| NDC Code | 68084-519-21 |
| Proprietary Name | LISINOPRIL AND HYDROCHLOROTHIAZIDE |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-519-21) > 10 TABLET in 1 BLISTER PACK (68084-519-11) |
| Product NDC | 68084-519 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LISINOPRIL AND HYDROCHLOROTHIAZIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130612 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
| Strength Number | 25; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
