Acetazolamide

Product NDC

55289-221

11-digit product format

552890221

Labeler code

55289

Product ID

55289-221_7bd52a08-4e06-7b60-e053-2a91aa0aae61

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acetazolamide

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA040195

Marketing category

ANDA

Marketing start

1997-05-28

Marketing end

0000-00-00

Substance

ACETAZOLAMIDE

Active strength

250 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record