61919-739 : Benazepril 20 mg Oral Tablet, Coated
NDC: | 61919-739 |
Labeler: | Direct_rx |
Product Type: | Human Prescription Drug |
Drug Name: | Benazepril |
Dosage Form: | Oral Tablet, Coated |
Application #: | ANDA076118 |
Rev. Date: |
Appearance:
Markings: | S;343 |
Shapes: |
Round |
Colors: |
Gray |
Size (mm): | 8 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 61919-739-90: 90 TABLET, COATED IN 1 BOTTLE (61919‑739‑90)
Active Ingredients:
- Benazepril Hydrochloride
Dosage Strength:
- 20 mg
Inactive Ingredients:
- Silicon Dioxide
- Crospovidone (15 Mpa.s At 5%)
- Hypromelloses
- Lactose Monohydrate
- Magnesium Stearate
- Polyethylene Glycol, Unspecified
- Starch, Corn
- Titanium Dioxide
- Carnauba Wax
- Triacetin
- Ferric Oxide Yellow
- Cellulose, Microcrystalline
- Polydextrose
- Ferrosoferric Oxide /
Pharmaceutical Classes:
- Angiotensin Converting Enzyme Inhibitor [EPC]
- Angiotensin-converting Enzyme Inhibitors [MoA]
- Decreased Blood Pressure [PE]
Related Products:
Based on records with the same trade name.- 16590-259 Bzp Hydrochloride 20 mg Oral Tablet by Stat Rx USA LLC
- 54458-893 Bzp Hydrochloride 40 mg Oral Tablet by International Labs, Inc.
NDC QR Code
Scan the QR code below to easily reference this data in the future:< Prev: 61919-737Next: 61919-741 >
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.