Ondansetron

Product NDC

70518-0892

11-digit product format

705180892

Labeler code

70518

Product ID

70518-0892_a5a21524-b61e-b99c-e053-2995a90ae6cf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ondansetron

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077851

Marketing category

ANDA

Marketing start

2017-12-12

Marketing end

0000-00-00

Substance

ONDANSETRON HYDROCHLORIDE

Active strength

4 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record