Lisinopril Tablets USP, 20 mg, 1000-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore MD 21202, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, India. NDC 68180-0981-03
Reported: April 29, 2020 Initiated: April 20, 2020 #D-1250-2020
Product Description
Lisinopril Tablets USP, 20 mg, 1000-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore MD 21202, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, India. NDC 68180-0981-03
Reason for Recall
Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril tablets inside of 2 sealed bottles of 20 mg/1000 count bottles.
Details
- Recalling Firm
- Lupin Pharmaceuticals Inc.
- Units Affected
- 11,808 bottles
- Distribution
- Product was distributed Nationwide in the United States.
- Location
- Baltimore, MD
Frequently Asked Questions
What product was recalled? ▼
Lisinopril Tablets USP, 20 mg, 1000-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore MD 21202, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, India. NDC 68180-0981-03. Recalled by Lupin Pharmaceuticals Inc.. Units affected: 11,808 bottles.
Why was this product recalled? ▼
Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril tablets inside of 2 sealed bottles of 20 mg/1000 count bottles.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 29, 2020. Severity: Moderate. Recall number: D-1250-2020.
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