NDC 51407-268
Niacin 1000 mg tablet, extended release
On the label: Golden State Medical Supply, Inc.. It's repackaged: Golden State Medical Supply, Inc. rebottles it from Lannett Company, Inc.'s NDC 62175-322.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Lannett Company, Inc. names for other drugs.
Repackaging site
- Golden State Medical Supply Inc., Camarillo, CA, United States · repackages it and relabels it
Recalls
- May 29, 2026 · Class II · Golden State Medical Supply Inc.
Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour timepoint.
Lots: Lots: GS065128, GS065844, GS066695, GS067432, GS067993, expires: 01/31/2027. - May 27, 2026 · Class II · Lannett Company Inc.
Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.
Lots: Lot #: 25282724A, Exp. Date 2027/01 - Oct 20, 2025 · Class II · Golden State Medical Supply Inc.
Failed Dissolution Specifications
Lots: Lot, expiry: GS044385, exp 10/2025 ; GS044979, exp 10/2025 ; GS045797, exp 12/2025 ; GS046415, exp 12/2025 ; GS047197, exp 02/2026 ; GS047786, exp 02/2026 ; GS048477, exp 02/2026 ; GS049480, exp 03/2026 ; GS048873, exp 03/2026 ; GS049733, exp 03/2026 ; GS050224, exp 03/2026 ; GS050721, e… - Oct 10, 2025 · Class II · Lannett Company Inc.
Failed Dissolution Specifications
Lots: Lot, expiry: 21264027A, Exp 10/30/2025; 22266446A, Exp 12/31/2025; 22266901A, Exp 02/28/2026; 22267553A, 22267554A, Exp 03/31/2026; 22267555A, Exp 02/28/2026; 22267992A, Exp 04/30/2026; 22267993A, 22267994A, Exp 05/31/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Niacin: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 1000 mg
- Approval
- ANDA ANDA203899
- On the market since
- Jun 16, 2017
- Package NDCs
51407-268-90- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2026
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