Lupin Pharmaceuticals Inc. recalls Cefprozil for Oral Suspension USP, 250mg/5mL, packaged as a) 50 mL (when mixed) bottles (NDC 68180-402-01); b) 75 mL
Lupin Pharmaceuticals recalls Cefprozil oral suspension (250mg/5mL) due to superpotent drug hazard. Affected bottles (50mL, 75mL, 100mL) with specific NDCs and lot numbers. Contact for return instructions.
Recall notice
Superpotent Drug
Contact the company & request your remedy
What happened, in plain English
Lupin Pharmaceuticals is recalling Cefprozil oral suspension (250mg/5mL) because it contains a superpotent drug that could cause harm if misused. This recall affects specific bottle sizes and lot numbers sold through pharmacies. Read more at govinfonow.com/recall/36245-lupin-cefprozil-oral-suspension-recall-superpotent-drug-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/36245-lupin-cefprozil-oral-suspension-recall-superpotent-drug-risk · Updated October 4, 2026 · FDA enforcement record: FDA #D-0332-2021
Cite this page
“Lupin Cefprozil Oral Suspension Recall: Superpotent Drug Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36245-lupin-cefprozil-oral-suspension-recall-superpotent-drug-risk. Based on FDA recall #D-0332-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0332-2021%22&limit=1).
Why it’s dangerous
The recall is for a 'superpotent drug' hazard, meaning the medication could cause serious harm if not used correctly. However, the exact mechanism of how this leads to injury isn't specified in the record.
Who’s affected
People who have the recalled Cefprozil oral suspension bottles (50mL, 75mL, or 100mL) with the specified NDC numbers and lot dates. Prescriptions for this medication are typically for adults or children under 18.
How to tell if you have this one
Check for bottles labeled 'Cefprozil for Oral Suspension USP, 250mg/5mL' with sizes 50mL, 75mL, or 100mL (when mixed). The NDC numbers are 68180-402-01, 68180-402-02, or 68180-402-03. Lot numbers F801122, F801123, or F801124 with expiration dates June 2021.
- Brand
Lupin- Category
Drug
What to do — step by step
Check Product Details
Identify the bottle size (50mL, 75mL, or 100mL), NDC number, and lot number to confirm if it's affected.
Questions people ask
Is this medication safe to use?
The recall states it has a 'superpotent drug' hazard, but does not specify if it's safe to use. The official notice does not provide details on safe usage conditions.
How do I know if my bottle is affected?
Check for bottles labeled 'Cefprozil for Oral Suspension USP, 250mg/5mL' with sizes 50mL, 75mL, or 100mL (when mixed), NDC numbers 68180-402-01, 68180-402-02, or 68180-402-03, and lot numbers F801122, F801123, or F801124.
What should I do if I have the recalled product?
The recall record does not specify any remedy or action steps for affected products.
Contact Lupin
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-0332-2021 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-0332-2021 from Lupin. 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-0332-2021 (March 26, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0332-2021 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.