Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.
Reported: June 28, 2017 Initiated: June 1, 2017 #D-0921-2017
Product Description
Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.
Reason for Recall
Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
Details
- Recalling Firm
- Lucid Pharma LLC
- Units Affected
- a) 44168 bottles; b) 24960 bottles
- Distribution
- Nationwide in the USA
- Location
- East Brunswick, NJ
Frequently Asked Questions
What product was recalled? ▼
Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.. Recalled by Lucid Pharma LLC. Units affected: a) 44168 bottles; b) 24960 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 28, 2017. Severity: Moderate. Recall number: D-0921-2017.
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