Diamox Sequels

Product NDC

51285-754

11-digit product format

512850754

Labeler code

51285

Product ID

51285-754_da05ccb3-2c45-44b4-8696-e476753c103b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acetazolamide

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Teva Women's Health, Inc.

Application

NDA012945

Marketing category

NDA

Marketing start

2000-02-22

Marketing end

2019-05-31

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