NDC 53808-0809
Viracept 625 mg tablet, film coated
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Agouron's NDC 63010-027.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Manufacturing Deutschland GmbH | Freiburg im Breisgau, Germany | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 2, 2025 · 8 inspections |
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Makes the active ingredient, tests it and packages it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
Recalls
- Jul 8, 2014 · Class III · Pfizer Inc.
Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled with an incorrect expiry date 11/2016. The correct expiry date is 09/2016.
Lots: Lot H45241, exp. 11/16
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Nelfinavir: every company that makes it
- Form
- tablet, film coated
- Strength
- 625 mg
- Approval
- NDA NDA021503
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0809-1- Official label
- DailyMed (National Library of Medicine), updated Apr 13, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?