Olopatadine Hydrochloride

Product NDC

50090-3384

11-digit product format

500903384

Labeler code

50090

Product ID

50090-3384_9d4eb208-f098-4447-a007-76e1bb21e9ab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olopatadine Hydrochloride

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

A-S Medication Solutions

Application

ANDA078350

Marketing category

ANDA

Marketing start

2015-12-07

Marketing end

0000-00-00

Substance

OLOPATADINE HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record