Tretinoin Gel Microsphere

Product NDC

66530-259

11-digit product format

665300259

Labeler code

66530

Product ID

66530-259_0fd10595-1ff5-450c-8d0f-8d46b54959f7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tretinoin

Dosage form

GEL

Route

TOPICAL

Labeler

Spear Dermatology Products Inc

Application

NDA020475

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-10-01

Marketing end

2020-04-30

Substance

TRETINOIN

Active strength

0 mg/g

Pharmacologic classes

Retinoid [EPC],Retinoids [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record