NDC 52959-289
Viracept 250 mg tablet, film coated
On the label: H.J. Harkins Co., Inc.. It's repackaged: H.J. Harkins Co., Inc. rebottles it from Agouron's NDC 63010-010.
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
- 250 mg
- Approval
- NDA NDA020779
- On the market since
- Mar 14, 1997
- Package NDCs
52959-289-0652959-289-30- Official label
- DailyMed (National Library of Medicine), updated Apr 18, 2012
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