NDC 65862-308
Fosinopril Sodium and Hydrochlorothiazide 10 mg / 12.5 mg tablet
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Fosinoprilat and Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg / 12.5 mg
- Approval
- ANDA ANDA079245
- On the market since
- Jul 9, 2009
- Package NDCs
65862-308-0165862-308-3065862-308-99- Official label
- DailyMed (National Library of Medicine), updated Apr 28, 2024
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