Mckesson Packaging Services recalls RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY
Mckesson Packaging Services recalls 150mg RANITIDINE tablets (NDC 63739-489-10) due to failed stability specifications. These RX-only tablets, manufactured by Amneal Pharmaceuticals, may degrade over time.
Lower-risk recall
Failed Stability Specifications
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What happened, in plain English
Mckesson Packaging Services has recalled 150mg RANITIDINE tablets (NDC 63739-489-10) because they failed stability tests. This means the tablets could degrade over time, potentially affecting their effectiveness or safety. Read more at govinfonow.com/recall/40798-mckesson-ranitidine-tablets-150mg-recall-failed-stability-specifications.
Source Summary by GovInfoNow · govinfonow.com/recall/40798-mckesson-ranitidine-tablets-150mg-recall-failed-stability-specifications · Updated October 7, 2026 · FDA enforcement record: FDA #D-0914-2018
Cite this page
“Mckesson RANITIDINE Tablets 150mg Recall: Failed Stability Specifications.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40798-mckesson-ranitidine-tablets-150mg-recall-failed-stability-specifications. Based on FDA recall #D-0914-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0914-2018%22&limit=1).
Why it’s dangerous
The tablets failed stability specifications, meaning they may degrade over time. This could lead to reduced effectiveness or potential safety issues if the medication becomes unstable.
Who’s affected
Prescription drug users who have the specific RANITIDINE tablets with the listed lot numbers and expiration dates. Patients on long-term treatment with these tablets are most at risk.
How to tell if you have this one
Check for the product name 'RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10)', manufactured by Amneal Pharmaceuticals, with lot numbers 0113064, 0114628, 0115189, or 0115462 and expiration dates up to 08/2018.
- Brand
Mckesson Packaging Services- Category
Drug
What to do — step by step
Check Product Details
Verify the lot number and expiration date on the packaging to confirm if the product is affected.
Questions people ask
Why is this medication being recalled?
The tablets failed stability specifications, which means they may degrade over time and affect their effectiveness or safety.
How do I know if I have the recalled product?
Check for the product name 'RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10)', manufactured by Amneal Pharmaceuticals, with lot numbers 0113064, 0114628, 0115189, or 0115462 and expiration dates up to 08/2018.
What should I do if I have the recalled product?
The recall does not specify a remedy, so check with your healthcare provider or pharmacist for guidance.
Contact Mckesson Packaging Services
We’ve drafted a message you can send Mckesson Packaging Services to request your refund or repair — edit it as you like.
Subject: Recall D-0914-2018 — Mckesson Packaging Services Mckesson Packaging Services Hello, I own a Mckesson Packaging Services that is covered by recall D-0914-2018 from Mckesson Packaging Services. 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-0914-2018 (February 26, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0914-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.