NDC 50090-1723
Prezcobix 150 mg / 800 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Janssen Products LP's NDC 59676-575.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cilag AG | Schaffhausen, Switzerland | Makes the active ingredient | No problems foundNov 21, 2025 · 8 inspections |
| Gilead Alberta ULC | Edmonton, Canada | Makes the active ingredient | No problems foundMay 12, 2023 · 6 inspections |
| Janssen Ortho LLC | Gurabo, PR, United States | Makes it and tests it | Problems found, fixed voluntarilyMar 28, 2023 · 7 inspections |
| Janssen Pharmaceutical Sciences Unlimited Company | Co Cork, Ireland | Makes the active ingredient | Problems found, fixed voluntarilyOct 27, 2023 · 5 inspections |
| Patheon Inc. | Mississauga, Canada | Makes it and packages it | Problems found, fixed voluntarilyFeb 24, 2023 · 7 inspections |
| Porton Pharma Solutions Ltd | Chongqing, China | Makes the active ingredient | No problems foundMar 29, 2024 · 3 inspections |
| Thermo Fisher Scientific Cork Limited | Carrigaline, Ireland | Makes the active ingredient | Problems found, fixed voluntarilySep 7, 2022 · 6 inspections, 1 with FDA action |
| Yuhan Chemical Inc. | Ansan-si, South Korea | Makes the active ingredient | Problems found, fixed voluntarilyFeb 28, 2025 · 6 inspections |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Product details
- Generic drug
- Cobicistat and Darunavir: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 150 mg / 800 mg
- Approval
- NDA NDA205395
- On the market since
- Jan 31, 2015
- Package NDCs
50090-1723-0- Official label
- DailyMed (National Library of Medicine), updated Jan 2, 2024
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