Acetazolamide

Product NDC
51672-4023
11-digit product format
516724023
Labeler code
51672
Product ID
51672-4023_31e42345-2444-92e6-e063-6394a90ae741
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acetazolamide
Dosage form
TABLET
Route
ORAL
Labeler
Sun Pharmaceutical Industries, Inc.
Application
ANDA040195
Marketing category
ANDA
Marketing start
1997-05-28
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
2026-12-31
Current FDA listing
Yes

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
94b5d997-68ee-d92e-7c04-a34fdb427a66Product name920240509
d0adda24-c2d3-39f8-a845-ede9cd56b2c4Product name620210513
91efc97d-7785-4097-b6cf-4201369f41ebProduct name320190711

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-4023-1Acetazolamide100 in 1 BOTTLETABLET1007

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-4023-1EA - Each51672-402378633976-d9a5-42e5-883a-1151827e9d1f12012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-4023ACETAZOLAMIDE TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.]7Current NDC, Legacy NDC, 1 package rows20250406_abeb13eb-66a5-4030-9bc2-5981acd196b9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51672-4023-151672402301100 TABLET in 1 BOTTLE (51672-4023-1) 100 tablet1997-05-280000-00-00NoNoCurrent