spironolactone
Generic: spironolactone
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
spironolactone
Generic Name
spironolactone
Labeler
asclemed usa, inc.
Dosage Form
TABLET, COATED
Routes
Active Ingredients
spironolactone 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76420-926
Product ID
76420-926_2fa991e8-8594-6911-e063-6294a90a916d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040750
Listing Expiration
2026-12-31
Marketing Start
2021-01-04
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420926
Hyphenated Format
76420-926
Supplemental Identifiers
RxCUI
UNII
NUI
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
spironolactone (source: ndc)
Generic Name
spironolactone (source: ndc)
Application Number
ANDA040750 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 1000 TABLET, COATED in 1 BOTTLE (76420-926-00)
- 100 TABLET, COATED in 1 BOTTLE (76420-926-01)
- 500 TABLET, COATED in 1 BOTTLE (76420-926-05)
- 30 TABLET, COATED in 1 BOTTLE (76420-926-30)
- 60 TABLET, COATED in 1 BOTTLE (76420-926-60)
- 90 TABLET, COATED in 1 BOTTLE (76420-926-90)
Packages (6)
76420-926-00
1000 TABLET, COATED in 1 BOTTLE (76420-926-00)
76420-926-01
100 TABLET, COATED in 1 BOTTLE (76420-926-01)
76420-926-05
500 TABLET, COATED in 1 BOTTLE (76420-926-05)
76420-926-30
30 TABLET, COATED in 1 BOTTLE (76420-926-30)
76420-926-60
60 TABLET, COATED in 1 BOTTLE (76420-926-60)
76420-926-90
90 TABLET, COATED in 1 BOTTLE (76420-926-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2fa991e8-8594-6911-e063-6294a90a916d", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["db22e9e5-2d88-4712-a809-c00881edb447"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (76420-926-00)", "package_ndc": "76420-926-00", "marketing_start_date": "20250306"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (76420-926-01)", "package_ndc": "76420-926-01", "marketing_start_date": "20250306"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (76420-926-05)", "package_ndc": "76420-926-05", "marketing_start_date": "20250306"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (76420-926-30)", "package_ndc": "76420-926-30", "marketing_start_date": "20250306"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (76420-926-60)", "package_ndc": "76420-926-60", "marketing_start_date": "20250306"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (76420-926-90)", "package_ndc": "76420-926-90", "marketing_start_date": "20250306"}], "brand_name": "Spironolactone", "product_id": "76420-926_2fa991e8-8594-6911-e063-6294a90a916d", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "76420-926", "generic_name": "Spironolactone", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA040750", "marketing_category": "ANDA", "marketing_start_date": "20210104", "listing_expiration_date": "20261231"}