NDC 68180-153 – Desloratadine

Desloratadine 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC68180-153

Product details

Brand name
Desloratadine
Generic name
Desloratadine
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078352
Marketed since
February 25, 2013
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Desloratadine →

Package NDC codes (2)

Package NDCDescriptionSince
68180-153-01100 TABLET, FILM COATED in 1 BOTTLE (68180-153-01)Feb 25, 2013
68180-153-02500 TABLET, FILM COATED in 1 BOTTLE (68180-153-02)Feb 25, 2013

Recalls mentioning this NDC

Other Desloratadine products