NDC 55111-153 – Ondansetron

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

Human Prescription Drug

Product NDC55111-153

Product details

Brand name
Ondansetron
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 →

Package NDC codes (5)

Package NDCDescriptionSince
55111-153-01100 TABLET, FILM COATED in 1 BOTTLE (55111-153-01)Dec 26, 2006
55111-153-05500 TABLET, FILM COATED in 1 BOTTLE (55111-153-05)Dec 26, 2006
55111-153-133 DOSE PACK in 1 BOX (55111-153-13) / 1 TABLET, FILM COATED in 1 DOSE PACKDec 26, 2006
55111-153-3030 TABLET, FILM COATED in 1 BOTTLE (55111-153-30)Dec 26, 2006
55111-153-7810 DOSE PACK in 1 BOX (55111-153-78) / 10 TABLET, FILM COATED in 1 DOSE PACKDec 26, 2006

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