NDC 68462-105 – Ondansetron

Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC68462-105

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077535
Marketed since
June 25, 2007
Listing expires
December 31, 2027
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron →

Package NDC codes (2)

Package NDCDescriptionSince
68462-105-3030 TABLET, FILM COATED in 1 BOTTLE (68462-105-30)Jun 25, 2007
68462-105-331 BLISTER PACK in 1 CARTON (68462-105-33) / 3 TABLET, FILM COATED in 1 BLISTER PACKJun 25, 2007

Recalls mentioning this NDC

Other Ondansetron products