desonide

Product NDC

69007-770

11-digit product format

690070770

Labeler code

69007

Product ID

69007-770_5fb0f21a-0f62-4aeb-a02e-cbbf2c32c784

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

desonide

Dosage form

CREAM

Route

TOPICAL

Labeler

Owen Laboratories, Inc.

Application

NDA019048

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

1984-12-14

Marketing end

0000-00-00

Substance

DESONIDE

Active strength

1 mg/g

Pharmacologic classes

Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record