Suprax (cefixime for oral suspension) USP, 100 mg/5 mL, 50 mL bottles (when reconstituted), Manufactured for Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, MD 21202, Manufactured by Lupin Limited Mumbai 400 058 India, NDC 68180-202-03.
Reported: April 24, 2013 Initiated: January 31, 2013 #D-264-2013
Product Description
Suprax (cefixime for oral suspension) USP, 100 mg/5 mL, 50 mL bottles (when reconstituted), Manufactured for Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, MD 21202, Manufactured by Lupin Limited Mumbai 400 058 India, NDC 68180-202-03.
Reason for Recall
Discoloration; Product may not meet specifications for color description once reconstituted.
Details
- Recalling Firm
- Lupin Pharmaceuticals Inc.
- Units Affected
- 64,368 bottles
- Distribution
- Nationwide
- Location
- Baltimore, MD
Frequently Asked Questions
What product was recalled? ▼
Suprax (cefixime for oral suspension) USP, 100 mg/5 mL, 50 mL bottles (when reconstituted), Manufactured for Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, MD 21202, Manufactured by Lupin Limited Mumbai 400 058 India, NDC 68180-202-03.. Recalled by Lupin Pharmaceuticals Inc.. Units affected: 64,368 bottles.
Why was this product recalled? ▼
Discoloration; Product may not meet specifications for color description once reconstituted.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 24, 2013. Severity: Low. Recall number: D-264-2013.
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