Tretinoin

Product NDC

43478-245

11-digit product format

434780245

Labeler code

43478

Product ID

43478-245_a61787f3-f3c8-4ea7-b659-f1ba1655336b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

tretinoin

Dosage form

GEL

Route

TOPICAL

Labeler

Rouses Point

Application

ANDA075589

Marketing category

ANDA

Marketing start

2002-06-11

Marketing end

2019-05-01

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