Acetazolamide

Product NDC

68084-401

11-digit product format

680840401

Labeler code

68084

Product ID

68084-401_82ce2492-b3b3-54a3-e053-2a91aa0a023e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acetazolamide

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

American Health Packaging

Application

ANDA040904

Marketing category

ANDA

Marketing start

2010-02-15

Marketing end

2020-08-31

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