NDC 55111-155 – Ondansetron hydrochloride

Ondansetron Hydrochloride 16 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC55111-155

Product details

Brand name
Ondansetron hydrochloride
Generic name
Ondansetron hydrochloride
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076183
Marketed since
December 26, 2006
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-3 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Ondansetron hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
55111-155-05500 TABLET, FILM COATED in 1 BOTTLE (55111-155-05)Dec 26, 2006
55111-155-3030 TABLET, FILM COATED in 1 BOTTLE (55111-155-30)Dec 26, 2006
55111-155-7810 BLISTER PACK in 1 CARTON (55111-155-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-155-79)Dec 26, 2006

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