TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21
Reported: January 11, 2017 Initiated: December 22, 2016 #D-0326-2017
Product Description
TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21
Reason for Recall
Failed Stability Specifications
Details
- Recalling Firm
- Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals
- Units Affected
- 1200 bottles
- Distribution
- Nationwide
- Location
- Huntsville, AL
Frequently Asked Questions
What product was recalled? ▼
TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21. Recalled by Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals. Units affected: 1200 bottles.
Why was this product recalled? ▼
Failed Stability Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 11, 2017. Severity: Low. Recall number: D-0326-2017.
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