Candesartan Cilexetil-Hydrochlorothiazide - Candesartan Cilexetil and Hydrochlorothiazide
Navigation: NDC > Supplier starting with: P > PAR PHARMACEUTICAL INC.| Field | Value |
|---|---|
| NDC Code: | 49884-662 |
| Proprietary Name: | Candesartan Cilexetil-Hydrochlorothiazide |
| Suffix: | |
| Non-Proprietary Name: | Candesartan Cilexetil and Hydrochlorothiazide |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 05-12-2012 |
| Category Name: | NDA AUTHORIZED GENERIC |
| Application Number: | NDA021093 |
| Labeler: | PAR PHARMACEUTICAL INC. |
| Substance Name: | CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: | 16; 12.5 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |