TRETINOIN

Product NDC

68788-7039

11-digit product format

687887039

Labeler code

68788

Product ID

68788-7039_f16a2b5f-cfb6-4a38-b36f-216241c40d78

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

tretinoin

Dosage form

CREAM

Route

TOPICAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA075265

Marketing category

ANDA

Marketing start

2017-10-27

Marketing end

0000-00-00

Substance

TRETINOIN

Active strength

1 mg/g

Pharmacologic classes

Retinoid [EPC],Retinoids [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record