70518-3172 : Benazepril Hydrochloride 20 mg Oral Tablet, Film Coated
NDC: | 70518-3172 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Benazepril Hydrochloride |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA078212 |
Rev. Date: |
NDC Package Codes:
- 70518-3172-0: 30 TABLET, FILM COATED IN 1 BLISTER PACK (70518‑3172‑0)
Active Ingredients:
- Benazepril Hydrochloride
Dosage Strength:
- 20 mg
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.- 70518-0216 Benazepril Hydrochloride 10 mg Oral Tablet by Remedyrepack Inc.
- 70518-0252 Benazepril Hydrochloride 10 mg Oral Tablet, Coated by Remedyrepack Inc.
- 70518-1640 Benazepril Hydrochloride 20 mg Oral Tablet, Coated by Remedyrepack Inc.
- 70518-1700 Benazepril Hydrochloride 40 mg Oral Tablet, Coated by Remedyrepack Inc.
- 70518-2125 Benazepril Hydrochloride 40 mg Oral Tablet, Coated by Remedyrepack Inc.
- 70518-3074 Benazepril Hydrochloride 10 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-3171 Benazepril Hydrochloride 40 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-3528 Benazepril Hydrochloride 20 mg Oral Tablet by Remedyrepack Inc.
- 49349-302 Bzp Hydrochloride 20 mg Oral Tablet by Remedyrepack Inc.
- 61786-336 Benazepril Hydrochloride 10 mg Oral Tablet, Coated by Remedyrepack Inc.
- 61786-343 Benazepril Hydrochloride 20 mg Oral Tablet, Coated by Remedyrepack Inc.
- 61786-669 Benazepril Hydrochloride 10 mg Oral Tablet by Remedyrepack Inc.
- 61786-784 Benazepril Hydrochloride 20 mg Oral Tablet, Coated by Remedyrepack Inc.
- 0093-5124 Bzp Hydrochloride 5 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-5125 Bzp Hydrochloride 10 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-5126 Bzp Hydrochloride 20 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0093-5127 Bzp Hydrochloride 40 mg Oral Tablet by Teva Pharmaceuticals USA Inc
- 0185-0048 Bzp Hydrochloride 40 mg Oral Tablet by Eon Labs, Inc.
- 0185-0053 Bzp Hydrochloride 10 mg Oral Tablet by Eon Labs, Inc.
- 0185-0505 Bzp Hydrochloride 5 mg Oral Tablet by Eon Labs, Inc.
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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.