FDA NDC
Benazepril Hydrochloride and Hydrochlorothiazide
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 62559-416
- Proprietary name
- Benazepril Hydrochloride and Hydrochlorothiazide
- Nonproprietary name
- Benazepril Hydrochloride and Hydrochlorothiazide
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Strength
- 20 mg/1
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