Tamoxifen Citrate

Product NDC

51862-450

11-digit product format

518620450

Labeler code

51862

Product ID

51862-450_119f75fc-b5e9-4a34-93d1-99ac302ac545

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tamoxifen Citrate

Dosage form

TABLET

Route

ORAL

Labeler

Mayne Pharma Inc.

Application

ANDA070929

Marketing category

ANDA

Marketing start

2016-07-18

Marketing end

2019-07-31

Substance

TAMOXIFEN CITRATE

Active strength

20 mg/1

Pharmacologic classes

Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record