NDC 71205-049
Allopurinol 300 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Accord Healthcare Inc.'s NDC 16729-135.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Intas Pharmaceuticals Limited | Ahmedabad, India | Makes it and tests it | No problems foundJul 12, 2024 · 10 inspections |
| Intas Pharmaceuticals Limited | Ahmedabad, India | Makes it and tests it | Serious problems, FDA actionDec 2, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Recalls
- Jan 12, 2023 · Class II · Accord Healthcare, Inc.
Presence of Foreign Substance: Presence of a small piece of green plastic embedded in the crack towards the edge of the tablet.
Lots: Lots: R2200455, R2200456 Exp. 03/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Allopurinol: every company that makes it
- Form
- tablet, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA203154
- On the market since
- Apr 29, 2015
- Package NDCs
71205-049-3071205-049-6071205-049-90- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?