Benazepril Hydrochloride - benazepril hydrochloride
Navigation: NDC > Supplier starting with: R > RANBAXY PHARMACEUTICALS INC.| Field | Value |
|---|---|
| NDC Code: | 63304-736 |
| Proprietary Name: | Benazepril Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | benazepril hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 11-02-2004 |
| Category Name: | ANDA |
| Application Number: | ANDA076344 |
| Labeler: | RANBAXY PHARMACEUTICALS INC. |
| Substance Name: | BENAZEPRIL HYDROCHLORIDE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
| DEA Schedule: |