spironolactone
Generic: spironolactone
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
spironolactone
Generic Name
spironolactone
Labeler
a-s medication solutions
Dosage Form
TABLET, COATED
Routes
Active Ingredients
spironolactone 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6600
Product ID
50090-6600_49b3e189-6f4f-4443-a50a-e837db477c14
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
500906600
Hyphenated Format
50090-6600
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
- 90 TABLET, COATED in 1 BOTTLE (50090-6600-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49b3e189-6f4f-4443-a50a-e837db477c14", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["15641f17-a08e-432b-ab8f-13db623e612e"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-6600-0)", "package_ndc": "50090-6600-0", "marketing_start_date": "20230821"}], "brand_name": "Spironolactone", "product_id": "50090-6600_49b3e189-6f4f-4443-a50a-e837db477c14", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "50090-6600", "generic_name": "Spironolactone", "labeler_name": "A-S Medication Solutions", "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"}