Meclizine hydrochloride tablets USP recall
Meclizine hydrochloride tablets USP, 12.5 mg, 100 count HDPE bottle, Rx only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD…
Why was Meclizine hydrochloride tablets USP recalled?
Marketed without an approved NDA/ANDA: Bottles were released prior to final approval.
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 # 17P0430, Exp 05/19
- Product
- Meclizine hydrochloride tablets USP, 12.5 mg, 100 count HDPE bottle, Rx only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD…
- Recalling firm
- Jubilant Cadista Pharmaceuticals, Inc.
- Quantity
- 744 bottles
- Distribution
- Nationwide
- Recall date
- November 22, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)