ethacrynic acid

Generic: ethacrynic acid

Labeler: sciegen pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ethacrynic acid
Generic Name ethacrynic acid
Labeler sciegen pharmaceuticals inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ethacrynic acid 25 mg/1

Manufacturer
ScieGen Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 50228-334
Product ID 50228-334_2a0ab1c4-a5f5-aeed-e063-6394a90a5992
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211232
Listing Expiration 2026-12-31
Marketing Start 2019-08-27

Pharmacologic Class

Established (EPC)
loop diuretic [epc]
Physiologic Effect
increased diuresis at loop of henle [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50228334
Hyphenated Format 50228-334

Supplemental Identifiers

RxCUI
1251903
UPC
0350228334013 0350228334303 0350228334105
UNII
M5DP350VZV
NUI
N0000175366 N0000175590

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 ethacrynic acid (source: ndc)
Generic Name ethacrynic acid (source: ndc)
Application Number ANDA211232 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (50228-334-01)
  • 100 TABLET in 1 BOTTLE (50228-334-10)
  • 30 TABLET in 1 BOTTLE (50228-334-30)
source: ndc

Packages (3)

Ingredients (1)

ethacrynic acid (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a0ab1c4-a5f5-aeed-e063-6394a90a5992", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0350228334013", "0350228334303", "0350228334105"], "unii": ["M5DP350VZV"], "rxcui": ["1251903"], "spl_set_id": ["d400d264-c231-4bdf-8180-eb11ab4e9f29"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["ScieGen Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-334-01)", "package_ndc": "50228-334-01", "marketing_start_date": "20190827"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50228-334-10)", "package_ndc": "50228-334-10", "marketing_start_date": "20190827"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-334-30)", "package_ndc": "50228-334-30", "marketing_start_date": "20190827"}], "brand_name": "Ethacrynic Acid", "product_id": "50228-334_2a0ab1c4-a5f5-aeed-e063-6394a90a5992", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50228-334", "generic_name": "Ethacrynic Acid", "labeler_name": "ScieGen Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ethacrynic Acid", "active_ingredients": [{"name": "ETHACRYNIC ACID", "strength": "25 mg/1"}], "application_number": "ANDA211232", "marketing_category": "ANDA", "marketing_start_date": "20190827", "listing_expiration_date": "20261231"}