Tretinoin Gel

Product NDC

66530-262

11-digit product format

665300262

Labeler code

66530

Product ID

66530-262_3c68cdba-d1b2-40f7-9a9d-1d770141bbe8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tretinoin

Dosage form

GEL

Route

TOPICAL

Labeler

Spear Dermatology Products

Application

ANDA207955

Marketing category

ANDA

Marketing start

2015-09-01

Marketing end

2019-07-31

Substance

TRETINOIN

Active strength

0 g/100g

Pharmacologic classes

Retinoid [EPC],Retinoids [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record