NDC 13811-630
BENAZEPRIL HYDROCHLORIDE
Benazepril Hydrochloride
BENAZEPRIL HYDROCHLORIDE is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Trigen Laboratories, Inc.. The primary component is Benazepril Hydrochloride.
Product ID | 13811-630_df70c619-a81f-48c3-8ec7-0135dc1fb450 |
NDC | 13811-630 |
Product Type | Human Prescription Drug |
Proprietary Name | BENAZEPRIL HYDROCHLORIDE |
Generic Name | Benazepril Hydrochloride |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2012-11-15 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA076118 |
Labeler Name | Trigen Laboratories, Inc. |
Substance Name | BENAZEPRIL HYDROCHLORIDE |
Active Ingredient Strength | 40 mg/1 |
Pharm Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |