NDC 51407-638
Primidone 250 mg tablet
On the label: Golden State Medical Supply, Inc.. It's repackaged: Golden State Medical Supply, 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
- Golden State Medical Supply Inc., Camarillo, CA, United States · repackages it and relabels it
Recalls
- Apr 27, 2026 · Class III · Golden State Medical Supply Inc.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Lots: Lot#: GS066750, GS067084, GS067710, GS067873, Exp 3/31/2028; GS068339, GS068897, Exp 8/31/2028 - Apr 27, 2026 · Class III · Golden State Medical Supply Inc.
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Lots: Lot #: GS067909, Exp 4/30/2028; GS068646, Exp 8/31/2026 - 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, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA084903
- On the market since
- Dec 1, 1978
- Package NDCs
51407-638-01- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2024
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