NDC 63304-404
Fosinopril Sodium and Hydrochlorothiazide 20 mg / 12.5 mg tablet
On the label: Ranbaxy Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ranbaxy Laboratories Limited - Dewas | Location not on file | Makes it | Not inspected on record |
Product details
- Generic drug
- Fosinoprilat and Hydrochlorothiazide: every company that makes it
- Form
- tablet
- Strength
- 20 mg / 12.5 mg
- Approval
- ANDA ANDA076739
- On the market since
- Dec 20, 2004
- Package NDCs
63304-404-0163304-404-1063304-404-30- Official label
- DailyMed (National Library of Medicine), updated Nov 10, 2013
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