FDA-Drug2018-05-30Class II

PrednisoLONE Sodium Phosphate Orally Disintegrating Tablets, 30 mg, Rx Only, 48-count bottle, NDC 00378-4730-22

Mylan Pharmaceuticals Inc.
Hazard

CGMP Deviations

Sold states
Recalling firm distributed product to wholesalers throughout the United States, including Puerto Rico.
Affected count
3,844 48-count bottles
Manufactured in
781 Chestnut Ridge Rd, N/A, Morgantown, WV, United States
Products
PrednisoLONE Sodium Phosphate Orally Disintegrating Tablets, 30 mg, Rx Only, 48-count bottle, NDC 00378-4730-22

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0831-2018

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief