Lustra-AF

Product NDC

51672-1327

11-digit product format

516721327

Labeler code

51672

Product ID

51672-1327_a9ea50e1-ec17-4342-80f5-7bc6d7bc8cb9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydroquinone

Dosage form

CREAM

Route

TOPICAL

Labeler

Taro Pharmaceuticals U.S.A., Inc.

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2005-01-20

Marketing end

0000-00-00

Substance

HYDROQUINONE

Active strength

40 mg/g

Pharmacologic classes

Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Depigmenting Activity [PE]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record