ALBENZA

Product NDC

65084-462

11-digit product format

650840462

Labeler code

65084

Product ID

65084-462_e5029392-88d4-44fd-b863-5570459db3fb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

albendazole

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mckesson Rxpak Inc

Application

NDA020666

Marketing category

NDA

Marketing start

1996-06-11

Marketing end

0000-00-00

Substance

ALBENDAZOLE

Active strength

200 mg/1

Pharmacologic classes

Anthelmintic [EPC],Cytochrome P450 1A Inducers [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record