Methylphenidate Hydrochloride Extended-release Tablets recall: Subpotent
Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC…
Why was Methylphenidate Hydrochloride Extended-release Tablets recalled?
Subpotent Drug
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 170027A, Exp. 02/2019
- Product
- Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC…
- Recalling firm
- Osmotica Pharmaceutical Corp
- Quantity
- 10064 bottles
- Distribution
- Nationwide
- Recall date
- December 27, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)