ondansetron

Product NDC

68071-4529

11-digit product format

680714529

Labeler code

68071

Product ID

68071-4529_737d1518-cb97-3fb9-e053-2a91aa0a7684

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ondansetron hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA077851

Marketing category

ANDA

Marketing start

2007-06-25

Marketing end

0000-00-00

Substance

ONDANSETRON HYDROCHLORIDE

Active strength

8 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record