Uniretic - moexipril hydrochloride and hydrochlorothiazide
Navigation: NDC > Supplier starting with: U > UCB, INC.| Field | Value |
|---|---|
| NDC Code: | 0091-3712 |
| Proprietary Name: | Uniretic |
| Suffix: | |
| Non-Proprietary Name: | moexipril hydrochloride and hydrochlorothiazide |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 15-09-1997 |
| Category Name: | NDA |
| Application Number: | NDA020729 |
| Labeler: | UCB, INC. |
| Substance Name: | HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE |
| Active Numerator Strength: | 12.5; 7.5 |
| 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: |