NDC 68462-157 – Ondansetron

Ondansetron 4 mg/1 · Tablet, Orally Disintegrating · Oral

Human Prescription Drug 1 recall

Product NDC68462-157

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet, Orally Disintegrating
Route
Oral
Marketing category
ANDA · ANDA078152
Marketed since
June 27, 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 (1)

Package NDCDescriptionSince
68462-157-1330 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (68462-157-13)Jun 27, 2007

Recalls mentioning this NDC

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