Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3
Reported: January 26, 2022 Initiated: January 10, 2022 #D-0388-2022
Product Description
Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3
Reason for Recall
Subpotent drug
Details
- Recalling Firm
- Dr. Reddy's Laboratories, Inc.
- Units Affected
- 18336 cartons
- Distribution
- USA Nationwide
- Location
- Princeton, NJ
Frequently Asked Questions
What product was recalled? ▼
Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 18336 cartons.
Why was this product recalled? ▼
Subpotent drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 26, 2022. Severity: Low. Recall number: D-0388-2022.
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