Tretinoin

Product NDC

66530-255

11-digit product format

665300255

Labeler code

66530

Product ID

66530-255_9cdb4f42-7502-4cb2-b379-639fe4c776e6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tretinoin

Dosage form

CREAM

Route

TOPICAL

Labeler

Spear Dermatology Products Inc

Application

NDA017340

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-02-06

Marketing end

2020-06-27

Substance

TRETINOIN

Active strength

1 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