Acetazolamide

Product NDC

39822-0191

11-digit product format

398220191

Labeler code

39822

Product ID

39822-0191_8f8499bd-b08c-43a2-8699-8b82ba014ce5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acetazolamide

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

X-GEN Pharmaceuticals, Inc.

Application

ANDA040784

Marketing category

ANDA

Marketing start

2013-12-10

Marketing end

0000-00-00

Substance

ACETAZOLAMIDE SODIUM

Active strength

500 mg/5mL

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