Lisinopril and hydrochlorothiazide - Lisinopril and hydrochlorothiazide
Navigation: NDC > Supplier starting with: W > WATSON LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 0591-0861 |
| Proprietary Name: | Lisinopril and hydrochlorothiazide |
| Suffix: | |
| Non-Proprietary Name: | Lisinopril and hydrochlorothiazide |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 01-03-2003 |
| Category Name: | ANDA |
| Application Number: | ANDA076194 |
| Labeler: | WATSON LABORATORIES, INC. |
| Substance Name: | HYDROCHLOROTHIAZIDE; LISINOPRIL |
| Active Numerator Strength: | 12.5; 20 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |