NDC 0527-1050

AcetaZOLAMIDE

Acetazolamide

AcetaZOLAMIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Lannett Company, Inc.. The primary component is Acetazolamide.

Product ID0527-1050_84acb9aa-f9d1-442a-90f8-45e698638769
NDC0527-1050
Product TypeHuman Prescription Drug
Proprietary NameAcetaZOLAMIDE
Generic NameAcetazolamide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1978-03-31
Marketing CategoryANDA / ANDA
Application NumberANDA084840
Labeler NameLannett Company, Inc.
Substance NameACETAZOLAMIDE
Active Ingredient Strength250 mg/1
Pharm ClassesCarbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0527-1050-01

100 TABLET in 1 BOTTLE, PLASTIC (0527-1050-01)
Marketing Start Date1978-03-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0527-1050-01 [00527105001]

AcetaZOLAMIDE TABLET
Marketing CategoryANDA
Application NumberANDA084840
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1978-03-31

NDC 0527-1050-10 [00527105010]

AcetaZOLAMIDE TABLET
Marketing CategoryANDA
Application NumberANDA084840
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1978-03-31

NDC 0527-1050-05 [00527105005]

AcetaZOLAMIDE TABLET
Marketing CategoryANDA
Application NumberANDA084840
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1978-03-31

Drug Details

Active Ingredients

IngredientStrength
ACETAZOLAMIDE250 mg/1

OpenFDA Data

SPL SET ID:c1c76f21-e1fc-40ea-947a-bc9c752f80c8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197304
  • UPC Code
  • 0305271050014
  • Pharmacological Class

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

    NDC Crossover Matching brand name "AcetaZOLAMIDE" or generic name "Acetazolamide"

    NDCBrand NameGeneric Name
    0143-9006AcetaZOLAMIDEAcetazolamide
    0143-9503AcetaZOLAMIDEAcetazolamide
    0527-1050AcetaZOLAMIDEAcetazolamide
    0555-0513AcetazolamideAcetazolamide
    0615-1511AcetaZOLAMIDEAcetaZOLAMIDE
    0904-6663acetazolamideacetazolamide
    10135-567AcetaZOLAMIDEAcetazolamide
    10135-772AcetazolamideAcetazolamide
    10135-773AcetazolamideAcetazolamide
    16729-331acetazolamideacetazolamide
    23155-120acetazolamideacetazolamide
    23155-287acetazolamideacetazolamide
    23155-288acetazolamideacetazolamide
    23155-313AcetazolamideAcetazolamide
    23155-787AcetazolamideAcetazolamide
    23155-831AcetazolamideAcetazolamide
    25021-817Acetazolamideacetazolamide sodium
    29033-030AcetazolamideAcetazolamide
    39822-0190AcetazolamideAcetazolamide
    39822-0191AcetazolamideAcetazolamide
    42291-089acetazolamideacetazolamide
    42291-090acetazolamideacetazolamide
    68084-541AcetaZOLAMIDEAcetaZOLAMIDE
    68084-401AcetazolamideAcetazolamide
    68382-261ACETAZOLAMIDEACETAZOLAMIDE
    42291-103AcetaZOLAMIDEAcetaZOLAMIDE
    46708-349AcetazolamideAcetazolamide
    50090-0577AcetazolamideAcetazolamide
    50090-3003AcetaZOLAMIDEAcetaZOLAMIDE
    50090-0279AcetazolamideAcetazolamide
    50090-3132AcetazolamideAcetazolamide
    50742-233AcetazolamideAcetazolamide
    51672-4022AcetazolamideAcetazolamide
    51672-4023AcetazolamideAcetazolamide
    55289-720AcetazolamideAcetazolamide
    55289-221AcetazolamideAcetazolamide
    60429-033AcetazolamideAcetazolamide
    60429-034AcetazolamideAcetazolamide
    62332-349AcetazolamideAcetazolamide
    63629-7889acetazolamideacetazolamide
    64380-833AcetazolamideAcetazolamide
    64380-834AcetazolamideAcetazolamide
    67296-0801AcetaZOLAMIDEAcetaZOLAMIDE
    67457-853AcetazolamideAcetazolamide
    70710-1591acetazolamideacetazolamide
    50090-4511AcetazolamideAcetazolamide
    70954-034AcetazolamideAcetazolamide
    71205-308AcetazolamideAcetazolamide
    70954-033AcetazolamideAcetazolamide

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.