Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs ( 68180-723-10), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202
Reported: April 25, 2018 Initiated: March 27, 2018 #D-0684-2018
Product Description
Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs ( 68180-723-10), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202
Reason for Recall
Superpotent Drug
Details
- Recalling Firm
- Lupin Pharmaceuticals Inc.
- Units Affected
- 40,824 bottles
- Distribution
- Nationwide
- Location
- Baltimore, MD
Frequently Asked Questions
What product was recalled? ▼
Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs ( 68180-723-10), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202. Recalled by Lupin Pharmaceuticals Inc.. Units affected: 40,824 bottles.
Why was this product recalled? ▼
Superpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 25, 2018. Severity: Moderate. Recall number: D-0684-2018.
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