Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B, Morristown, NJ 07960. NDC: 45963-748-11.
Reported: April 13, 2016 Initiated: February 16, 2016 #D-0814-2016
Product Description
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B, Morristown, NJ 07960. NDC: 45963-748-11.
Reason for Recall
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Details
- Recalling Firm
- Actavis Elizabeth LLC
- Units Affected
- 257,746 Bottles
- Distribution
- US: Nationwide
- Location
- Elizabeth, NJ
Frequently Asked Questions
What product was recalled? ▼
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B, Morristown, NJ 07960. NDC: 45963-748-11.. Recalled by Actavis Elizabeth LLC. Units affected: 257,746 Bottles.
Why was this product recalled? ▼
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 13, 2016. Severity: Moderate. Recall number: D-0814-2016.
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