Cephalexin for Oral Suspension USP, 250 mg/5mL, 200 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Mumbai 400 098 INDIA, NDC 68180-0441-02
Reported: November 13, 2019 Initiated: November 1, 2019 #D-0304-2020
Product Description
Cephalexin for Oral Suspension USP, 250 mg/5mL, 200 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Mumbai 400 098 INDIA, NDC 68180-0441-02
Reason for Recall
Presence of Foreign substance: identified as a dead ant.
Details
- Recalling Firm
- Lupin Pharmaceuticals Inc.
- Units Affected
- 28,254 bottles
- Distribution
- Product was distributed to major distributors/wholesalers throughout the United States.
- Location
- Baltimore, MD
Frequently Asked Questions
What product was recalled? ▼
Cephalexin for Oral Suspension USP, 250 mg/5mL, 200 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Mumbai 400 098 INDIA, NDC 68180-0441-02. Recalled by Lupin Pharmaceuticals Inc.. Units affected: 28,254 bottles.
Why was this product recalled? ▼
Presence of Foreign substance: identified as a dead ant.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 13, 2019. Severity: Low. Recall number: D-0304-2020.
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