Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-ward Pharmaceutical Corp | Location not on file | Makes it, tests it and packages it | Not inspected on record |
| Apotheca Inc. | Phoenix, AZ, United States | Labels it and repackages it | No problems foundJan 8, 2025 · 6 inspections, 1 with FDA action |
Recalls
- Apr 20, 2017 · Class I · C. O. Truxton
Labeling: Label Mixup; potentially mislabeled
Lots: Lot # 70926A; Exp. 11/17 Lot # 70981A; Exp. 01/18 Lot # H15A59; Exp. 08/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Phenobarbital: every company that makes it
- Form
- tablet
- Strength
- 30 mg
- Approval
- UNAPPROVED DRUG OTHER
- On the market since
- Mar 1, 2012
- Package NDCs
0463-6145-010463-6145-10- Official label
- DailyMed (National Library of Medicine), updated Oct 17, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?