Bexarotene

Product NDC

42292-007

11-digit product format

422920007

Labeler code

42292

Product ID

42292-007_96261301-e766-3992-e053-2a95a90a1f54

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Bexarotene

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA203174

Marketing category

ANDA

Marketing start

2016-04-15

Marketing end

2020-01-31

Substance

BEXAROTENE

Active strength

75 mg/1

Pharmacologic classes

Retinoid [EPC],Retinoids [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record