GRANISETRON HYDROCHLORIDE

Product NDC

64679-841

11-digit product format

646790841

Labeler code

64679

Product ID

64679-841_d5c8408b-9f37-48c0-85f9-41620d0b220d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

GRANISETRON HYDROCHLORIDE

Dosage form

INJECTION

Route

INTRAVENOUS

Labeler

Wockhardt USA LLC.

Application

ANDA078565

Marketing category

ANDA

Marketing start

2008-06-30

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record