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Drug recall · FDA · Published October 26, 2020

Ascent Pharmaceuticals, Inc. recalls Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber

Ascent Pharmaceuticals recalls 100-count hydrocodone/acetaminophen tablets with foreign losartan tablets. Consumers should check product details and contact the company for guidance.

🇺🇸 FDA recall #D-0097-2021DrugAscent Pharmaceuticals ›
Take action

Contact the company & request your remedy

Recalling firmAscent Pharmaceuticals, Inc.400 S Technology Dr, N/A · Central Islip, NY 11722-4402
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Ascent Pharmaceuticals is recalling 100-count hydrocodone and acetaminophen tablets that contain a foreign losartan tablet. This could cause confusion or unintended medication use if the foreign tablet is taken. Read more at govinfonow.com/recall/36700-ascent-hydrocodone-tablets-recall-foreign-losartan-tablets-found.

Source Summary by GovInfoNow · govinfonow.com/recall/36700-ascent-hydrocodone-tablets-recall-foreign-losartan-tablets-found · Updated October 4, 2026 · FDA enforcement record: FDA #D-0097-2021

Cite this page

“Ascent Hydrocodone Tablets Recall: Foreign Losartan Tablets Found.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36700-ascent-hydrocodone-tablets-recall-foreign-losartan-tablets-found. Based on FDA recall #D-0097-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0097-2021%22&limit=1).

Why it’s dangerous

The tablets contain a foreign losartan tablet that could be mistaken for the intended medication. If taken, this could lead to unintended medication effects or interactions.

Who’s affected

Prescription owners of the specific 100-count hydrocodone/acetaminophen tablets with NDC 31722-943-01 and lot number 20070518. People taking the medication for pain or cough may be at risk if they accidentally consume the foreign losartan tablet.

How to tell if you have this one

Check for the NDC code 31722-943-01 and lot number 20070518 on the bottle. The product is a 100-count hydrocodone/acetaminophen tablet bottle manufactured for Camber Pharmaceuticals.

  • Brand
    Ascent Pharmaceuticals
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the NDC code 31722-943-01 and lot number 20070518 on the bottle.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product contains a foreign losartan tablet that could be mistaken for the intended medication, so it is not safe to use without checking.

How can I tell if I have the recalled product?

Check for the NDC code 31722-943-01 and lot number 20070518 on the bottle.

What should I do if I have the recalled product?

The recall does not specify a remedy, so contact Ascent Pharmaceuticals for guidance.

Take action

Contact Ascent Pharmaceuticals

We’ve drafted a message you can send Ascent Pharmaceuticals to request your refund or repair — edit it as you like.

Subject: Recall D-0097-2021 — Ascent Pharmaceuticals Ascent Pharmaceuticals

Hello,

I own a Ascent Pharmaceuticals that is covered by recall D-0097-2021 from Ascent Pharmaceuticals.

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-0097-2021 (October 26, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0097-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA