NDC 68788-8666 – Ondansetron

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

Human Prescription Drug 1 recall

Product NDC68788-8666

Product details

Brand name
Ondansetron
Generic name
Ondansetron
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Orally Disintegrating
Route
Oral
Marketing category
ANDA · ANDA078152
Marketed since
May 14, 2024
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
68788-8666-130 TABLET, ORALLY DISINTEGRATING in 1 PACKET (68788-8666-1)May 14, 2024
68788-8666-310 TABLET, ORALLY DISINTEGRATING in 1 BOX, UNIT-DOSE (68788-8666-3)May 14, 2024

Recalls mentioning this NDC

Other Ondansetron products