Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, Manufactured in Israel by: TEVA PHARMACEUTICALS IND. LTD. Jerusalem, 9777402, Israel, Manufactured for: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454, NDC 0093-7440-01.
Reported: August 3, 2016 Initiated: May 18, 2016 #D-1449-2016
Product Description
Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, Manufactured in Israel by: TEVA PHARMACEUTICALS IND. LTD. Jerusalem, 9777402, Israel, Manufactured for: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454, NDC 0093-7440-01.
Reason for Recall
Failed Tablet/Capsule Specifications
Details
- Recalling Firm
- Teva North America
- Units Affected
- 14, 370 units
- Distribution
- Nationwide and Puerto Rico
- Location
- Horsham, PA
Frequently Asked Questions
What product was recalled? ▼
Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, Manufactured in Israel by: TEVA PHARMACEUTICALS IND. LTD. Jerusalem, 9777402, Israel, Manufactured for: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454, NDC 0093-7440-01.. Recalled by Teva North America. Units affected: 14, 370 units.
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 3, 2016. Severity: Low. Recall number: D-1449-2016.
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