Ondansetron Hydrochloride 42708-0179-05

Package NDC

42708-0179-05

Manufacturer: Qpharma, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 31, 2007
Listing Expires: December 31, 2026
Application: ANDA078539

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Active Ingredients

Ingredient	Strength
Ondansetron Hydrochloride	8 mg/1

Drug Class

Serotonin 3 Receptor Antagonists [MoA]Serotonin-3 Receptor Antagonist [EPC]

Selected Package

42708-0179-05Selected

5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-179-05)