ANZEMET

Product NDC

30698-120

11-digit product format

306980120

Labeler code

30698

Product ID

30698-120_fc7a7002-d1d6-40f2-9a44-44ce51686152

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

dolasetron mesylate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Validus Pharmaceuticals LLC

Application

NDA020623

Marketing category

NDA

Marketing start

1997-09-11

Marketing end

0000-00-00

Substance

DOLASETRON MESYLATE

Active strength

50 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