acetazolamide

Generic: acetazolamide

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetazolamide
Generic Name acetazolamide
Labeler lifestar pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetazolamide 250 mg/1

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-721
Product ID 70756-721_a2eeb1bd-27f7-4323-a2de-69d456da08f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214282
Listing Expiration 2026-12-31
Marketing Start 2020-11-13

Pharmacologic Class

Established (EPC)
carbonic anhydrase inhibitor [epc]
Mechanism of Action
carbonic anhydrase inhibitors [moa]
Chemical Structure
sulfonamides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70756721
Hyphenated Format 70756-721

Supplemental Identifiers

RxCUI
197303 197304
UNII
O3FX965V0I
NUI
N0000175517 N0000000235 M0020790

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name acetazolamide (source: ndc)
Generic Name acetazolamide (source: ndc)
Application Number ANDA214282 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70756-721-11)
  • 10 BLISTER PACK in 1 CARTON (70756-721-99) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

70756-721-11 100 TABLET in 1 BOTTLE (70756-721-11) 70756-721-99 10 BLISTER PACK in 1 CARTON (70756-721-99) / 10 TABLET in 1 BLISTER PACK

Ingredients (1)

acetazolamide (250 mg/1)

Linked Drug Pages (1)

Acetazolamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a2eeb1bd-27f7-4323-a2de-69d456da08f0", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "unii": ["O3FX965V0I"], "rxcui": ["197303", "197304"], "spl_set_id": ["0913db35-3f08-4d82-8394-486bd9a487c4"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70756-721-11)", "package_ndc": "70756-721-11", "marketing_start_date": "20201113"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70756-721-99)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "70756-721-99", "marketing_start_date": "20240515"}], "brand_name": "Acetazolamide", "product_id": "70756-721_a2eeb1bd-27f7-4323-a2de-69d456da08f0", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "70756-721", "generic_name": "Acetazolamide", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE", "strength": "250 mg/1"}], "application_number": "ANDA214282", "marketing_category": "ANDA", "marketing_start_date": "20201113", "listing_expiration_date": "20261231"}