Venlafaxine Tablets, USP 50 mg*, 100 Tablets Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by: ALKALOIDA Chemical Company Zrt. 4440 Tiszavasvari, Kabay Janos u.29.Hungary. Product of India NDC 16714-657-01
Reported: August 18, 2021 Initiated: July 29, 2021 #D-0703-2021
Product Description
Venlafaxine Tablets, USP 50 mg*, 100 Tablets Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by: ALKALOIDA Chemical Company Zrt. 4440 Tiszavasvari, Kabay Janos u.29.Hungary. Product of India NDC 16714-657-01
Reason for Recall
Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg
Details
- Recalling Firm
- SUN PHARMACEUTICAL INDUSTRIES INC
- Units Affected
- 2856 bottles
- Distribution
- Northstar Distribution Center 4853 Crumpler Rd. Memphis, TN 38141
- Location
- Princeton, NJ
Frequently Asked Questions
What product was recalled? ▼
Venlafaxine Tablets, USP 50 mg*, 100 Tablets Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by: ALKALOIDA Chemical Company Zrt. 4440 Tiszavasvari, Kabay Janos u.29.Hungary. Product of India NDC 16714-657-01. Recalled by SUN PHARMACEUTICAL INDUSTRIES INC. Units affected: 2856 bottles.
Why was this product recalled? ▼
Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 18, 2021. Severity: Moderate. Recall number: D-0703-2021.
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