Tamoxifen Citrate

Product NDC

65084-269

11-digit product format

650840269

Labeler code

65084

Product ID

65084-269_50b20d45-f931-40ef-a599-d95c53da1fa5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tamoxifen Citrate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson Corporation dba RX Pak

Application

ANDA075797

Marketing category

ANDA

Marketing start

2016-08-03

Marketing end

0000-00-00

Substance

TAMOXIFEN CITRATE

Active strength

10 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record