Griseofulvin

Product NDC

68682-519

11-digit product format

686820519

Labeler code

68682

Product ID

68682-519_ab5a4a1c-90f1-40f3-aab4-6f299a885c52

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Griseofulvin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Oceanside Pharmaceuticals

Application

NDA050475

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2016-07-26

Marketing end

0000-00-00

Substance

GRISEOFULVIN

Active strength

125 mg/1

Pharmacologic classes

Decreased Mitosis [PE],Microtubule Inhibition [PE],Tubulin Inhibiting Agent [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record