Acetazolamide

Product NDC

0555-0513

11-digit product format

005550513

Labeler code

0555

Product ID

0555-0513_0d63cf21-a745-463c-a449-b716608062d3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acetazolamide

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

NDA012945

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2000-02-22

Marketing end

2019-06-30

Substance

ACETAZOLAMIDE

Active strength

500 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record