PlainRecalls
FDA Drug Low Class III Terminated

Clobetasol Propionate Foam (Emulsion Formulation), 0.05% a) 50 g pack (NDC 68462-625-27) and b) 100 g pack (NDC 68462-625-94), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited Plot No. B-25, MIDC, Shendra Aurangabad, Maharashtra -431210, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430

Reported: December 18, 2019 Initiated: November 15, 2019 #D-0619-2020

Product Description

Clobetasol Propionate Foam (Emulsion Formulation), 0.05% a) 50 g pack (NDC 68462-625-27) and b) 100 g pack (NDC 68462-625-94), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited Plot No. B-25, MIDC, Shendra Aurangabad, Maharashtra -431210, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430

Reason for Recall

Defective delivery system; product is not foaming or is coming out as liquid.

Details

Units Affected
a) 480 packs; b) 240 packs
Distribution
Nationwide
Location
Mahwah, NJ

Frequently Asked Questions

What product was recalled?
Clobetasol Propionate Foam (Emulsion Formulation), 0.05% a) 50 g pack (NDC 68462-625-27) and b) 100 g pack (NDC 68462-625-94), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited Plot No. B-25, MIDC, Shendra Aurangabad, Maharashtra -431210, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430. Recalled by Glenmark Pharmaceuticals Inc., USA. Units affected: a) 480 packs; b) 240 packs.
Why was this product recalled?
Defective delivery system; product is not foaming or is coming out as liquid.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 18, 2019. Severity: Low. Recall number: D-0619-2020.