55700-0627 Ondansetron Hydrochloride

Product NDC:

55700-0627

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 8.0

Unit: mg/1

Packages:

Code: 55700-0627-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE (55700-627-10)

Effective Date: May 18, 2018

Discontinued: June 30, 2027

Code: 55700-0627-12

Description: 12 TABLET, FILM COATED in 1 BOTTLE (55700-627-12)

Effective Date: May 18, 2018

Discontinued:

Code: 55700-0627-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (55700-627-20)

Effective Date: May 18, 2018

Discontinued: June 30, 2027

Code: 55700-0627-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (55700-627-30)

Effective Date: May 18, 2018

Discontinued: Jan. 31, 2028

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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