NDC 54868-2847
Quinapril Hydrochloride and Hydrochlorothiazide 12.5 mg / 20 nmol tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Ranbaxy Laboratories Inc.'s NDC 63304-162.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cambrex Profarmaco Milano SRL | Paullo, Italy | Makes the active ingredient | No problems foundNov 11, 2022 · 7 inspections, 1 with FDA action |
| Ohm Laboratories Inc. | North Brunswick, NJ, United States | Makes it and packages it | No problems foundOct 31, 2024 · 22 inspections |
| Ranbaxy laboratories Limited Toansa | Location not on file | Makes the active ingredient | Not inspected on record |
| Ohm Laboratories Inc. | New Brunswick, NJ, United States | Packages it | No problems foundOct 31, 2024 · 22 inspections |
Product details
- Generic drug
- Hydrochlorothiazide and Quinapril: every company that makes it
- Form
- tablet, film coated
- Strength
- 12.5 mg / 20 nmol
- Approval
- ANDA ANDA078211
- On the market since
- Aug 3, 2006
- Package NDCs
54868-2847-054868-2847-1- Official label
- DailyMed (National Library of Medicine), updated May 6, 2010
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