Dorzolamide Hydrochloride

Product NDC

0093-7618

11-digit product format

000937618

Labeler code

0093

Product ID

0093-7618_9b25de7a-7321-412b-8444-14b8a4eb2d4d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Dorzolamide Hydrochloride

Dosage form

SOLUTION

Route

OPHTHALMIC

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA078756

Marketing category

ANDA

Marketing start

2010-01-28

Marketing end

2019-05-31

Substance

DORZOLAMIDE HYDROCHLORIDE

Active strength

20 mg/mL

Pharmacologic classes

Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record