InvaGen Pharmaceuticals, Inc. recalls Gabapentin Tablets USP, 600 mg, Rx Only, 500-count bottle, Manufactured for: Exelan Pharmaceuticals, Inc.,
InvaGen Pharmaceuticals recalls 600mg Gabapentin tablets due to impurity failure in long-term stability testing. Affected lots may pose risks if stored beyond expiration.
Lower-risk recall
Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
Contact the company & request your remedy
What happened, in plain English
InvaGen Pharmaceuticals is recalling 600mg Gabapentin tablets that failed impurity tests during long-term stability testing. This could mean the tablets might contain harmful substances if stored past their expiration date. Read more at govinfonow.com/recall/37119-invagen-gabapentin-tablets-recall-impurity-risk-in-long-term-storage.
Source Summary by GovInfoNow · govinfonow.com/recall/37119-invagen-gabapentin-tablets-recall-impurity-risk-in-long-term-storage · Updated October 5, 2026 · FDA enforcement record: FDA #D-1272-2020
Cite this page
“InvaGen Gabapentin Tablets Recall: Impurity Risk in Long-Term Storage.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37119-invagen-gabapentin-tablets-recall-impurity-risk-in-long-term-storage. Based on FDA recall #D-1272-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1272-2020%22&limit=1).
Why it’s dangerous
The tablets failed a critical impurity test after 12 months of storage. This suggests the medication might contain harmful substances that could affect safety if used beyond the expiration date.
Who’s affected
Prescription users of the 600mg Gabapentin tablets with NDC 76282-405-05. Most at risk are those who have the specific lot number NB900413.
How to tell if you have this one
Check for the NDC code 76282-405-05 on the bottle. The specific lot number NB900413 was manufactured in Lawrenceville, GA and expires December 2020.
- Brand
InvaGen- Category
Drug
What to do — step by step
Check Product Details
Look for the NDC code 76282-405-05 and lot number NB900413 on the bottle.
Questions people ask
Is this product safe to use?
The recall indicates the product failed impurity tests during long-term stability testing, but the official notice does not specify if it is safe to use after the expiration date.
What should I do if I have this product?
The recall does not provide specific action steps for affected products, so the official notice does not say.
How can I tell if I have the recalled product?
Check for the NDC code 76282-405-05 and lot number NB900413 on the bottle.
Contact InvaGen
We’ve drafted a message you can send InvaGen to request your refund or repair — edit it as you like.
Subject: Recall D-1272-2020 — InvaGen InvaGen Hello, I own a InvaGen that is covered by recall D-1272-2020 from InvaGen. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1272-2020 (May 14, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1272-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.