Olopatadine Hydrochloride

Product NDC

68788-7403

11-digit product format

687887403

Labeler code

68788

Product ID

68788-7403_e1b5c905-7cc2-4b73-b894-ff56754b56a4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olopatadine Hydrochloride 0.1%

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA204706

Marketing category

ANDA

Marketing start

2016-10-10

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record