55111-0153 Ondansetron Hydrochloride

Product NDC:

55111-0153

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: Ondansetron Hydrochloride

Strength: 4.0

Unit: mg/1

Packages:

Code: 55111-0153-01

Description: 100 TABLET, FILM COATED in 1 BOTTLE (55111-153-01)

Effective Date: Dec. 26, 2006

Discontinued:

Code: 55111-0153-05

Description: 500 TABLET, FILM COATED in 1 BOTTLE (55111-153-05)

Effective Date: Dec. 26, 2006

Discontinued:

Code: 55111-0153-13

Description: 3 DOSE PACK in 1 BOX (55111-153-13) / 1 TABLET, FILM COATED in 1 DOSE PACK

Effective Date: Dec. 26, 2006

Discontinued:

Code: 55111-0153-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (55111-153-30)

Effective Date: Dec. 26, 2006

Discontinued:

Code: 55111-0153-78

Description: 10 DOSE PACK in 1 BOX (55111-153-78) / 10 TABLET, FILM COATED in 1 DOSE PACK

Effective Date: Dec. 26, 2006

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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