Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size), Powder for oral suspension, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore Maryland, Manufactured by: Lupin Limited, Mandideep, India NDC 68180-407-03
Reported: June 26, 2024 Initiated: May 30, 2024 #D-0559-2024
Product Description
Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size), Powder for oral suspension, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore Maryland, Manufactured by: Lupin Limited, Mandideep, India NDC 68180-407-03
Reason for Recall
Failed Content Uniformity Specifications
Details
- Recalling Firm
- Lupin Pharmaceuticals Inc.
- Units Affected
- 3,552 bottles
- Distribution
- Nationwide in the US
- Location
- Baltimore, MD
Frequently Asked Questions
What product was recalled? ▼
Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size), Powder for oral suspension, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore Maryland, Manufactured by: Lupin Limited, Mandideep, India NDC 68180-407-03. Recalled by Lupin Pharmaceuticals Inc.. Units affected: 3,552 bottles.
Why was this product recalled? ▼
Failed Content Uniformity Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 26, 2024. Severity: Moderate. Recall number: D-0559-2024.
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