granisetron hydrochloride

Product NDC

25021-779

11-digit product format

250210779

Labeler code

25021

Product ID

25021-779_56ebc9e3-daf4-4e96-9736-a51a30975dc4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

granisetron hydrochloride

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Sagent Pharmaceuticals

Application

ANDA091136

Marketing category

ANDA

Marketing start

2010-12-01

Marketing end

2019-06-01

Substance

GRANISETRON HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record