Ondansetron

Product NDC

70518-1422

11-digit product format

705181422

Labeler code

70518

Product ID

70518-1422_76cd7efa-d172-fd9e-e053-2a91aa0ad7b2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ondansetron hydrochloride

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

ANDA079224

Marketing category

ANDA

Marketing start

2018-09-18

Marketing end

0000-00-00

Substance

ONDANSETRON HYDROCHLORIDE

Active strength

2 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record