Latanoprost

Product NDC

0517-0830

11-digit product format

005170830

Labeler code

0517

Product ID

0517-0830_2db770c5-97b0-40dd-a442-d4d1be4f5df9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Latanoprost

Dosage form

SOLUTION

Route

OPHTHALMIC

Labeler

American Regent, Inc.

Application

ANDA200925

Marketing category

ANDA

Marketing start

2011-08-02

Marketing end

0000-00-00

Substance

LATANOPROST

Active strength

50 ug/mL

Pharmacologic classes

Prostaglandin Analog [EPC],Prostaglandins [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record