| NDC Code: |
49349-209 |
| Proprietary Name: |
Lisinopril and hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Lisinopril and hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
31-10-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA076194 |
| Labeler: |
REMEDYREPACK INC. |
| Substance Name: |
HYDROCHLOROTHIAZIDE; LISINOPRIL |
| Active Numerator Strength: |
12.5; 20 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
| DEA Schedule: |
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