NDC 54868-1691
Primidone 250 mg tablet
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Lannett Company, Inc.'s NDC 0527-1231.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Repackaging site
- Physicians Total Care, Inc., Tulsa, Oklahoma, United States · repackages it and relabels it
Recalls
- Apr 24, 2026 · Class III · Lannett Company Inc.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Lots: Lot#: 25283038A, Exp 1/31/2028; 25283564A, 25283565A, Exp 3/31/2028; 25285712A Exp 08/31/2028; 25284105A, Exp 4/30/2028; 25284874A, 25284875A, Exp 08/31/2028.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Primidone: every company that makes it
- Form
- tablet
- Strength
- 250 mg
- Approval
- ANDA ANDA084903
- On the market since
- Jul 27, 2009
- Package NDCs
54868-1691-054868-1691-254868-1691-354868-1691-454868-1691-5- Official label
- DailyMed (National Library of Medicine), updated Feb 19, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?