Epinastine Hydrochloride

Product NDC

50090-1635

11-digit product format

500901635

Labeler code

50090

Product ID

50090-1635_3592bbdc-acc8-40a6-b284-4fceca8ca464

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Epinastine Hydrochloride

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

A-S Medication Solutions

Application

ANDA090870

Marketing category

ANDA

Marketing start

2013-11-05

Marketing end

0000-00-00

Substance

EPINASTINE HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

Adrenergic Agonists [MoA],Adrenergic Receptor Agonist [EPC],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