Benazepril Hydrochloride - Benazepril Hydrochloride
Navigation: NDC > Supplier starting with: A > AUROBINDO PHARMA LIMITED| Field | Value |
|---|---|
| NDC Code: | 65862-117 |
| Proprietary Name: | Benazepril Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Benazepril Hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 22-05-2008 |
| Category Name: | ANDA |
| Application Number: | ANDA078212 |
| Labeler: | AUROBINDO PHARMA LIMITED |
| Substance Name: | BENAZEPRIL HYDROCHLORIDE |
| Active Numerator Strength: | 20 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
| DEA Schedule: |