spironolactone
Generic: spironolactone
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
spironolactone
Generic Name
spironolactone
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
spironolactone 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1627
Product ID
72162-1627_a6caa2b8-b27e-47eb-9db8-ccfa8e8b6a8b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089424
Listing Expiration
2027-12-31
Marketing Start
1986-07-23
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621627
Hyphenated Format
72162-1627
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
ANDA089424 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (72162-1627-1)
- 100 TABLET, FILM COATED in 1 BOTTLE (72162-1627-2)
- 30 TABLET, FILM COATED in 1 BOTTLE (72162-1627-3)
- 60 TABLET, FILM COATED in 1 BOTTLE (72162-1627-4)
- 500 TABLET, FILM COATED in 1 BOTTLE (72162-1627-5)
- 30 TABLET, FILM COATED in 1 BOTTLE (72162-1627-7)
Packages (6)
72162-1627-1
100 TABLET, FILM COATED in 1 BOTTLE (72162-1627-1)
72162-1627-2
100 TABLET, FILM COATED in 1 BOTTLE (72162-1627-2)
72162-1627-3
30 TABLET, FILM COATED in 1 BOTTLE (72162-1627-3)
72162-1627-4
60 TABLET, FILM COATED in 1 BOTTLE (72162-1627-4)
72162-1627-5
500 TABLET, FILM COATED in 1 BOTTLE (72162-1627-5)
72162-1627-7
30 TABLET, FILM COATED in 1 BOTTLE (72162-1627-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a6caa2b8-b27e-47eb-9db8-ccfa8e8b6a8b", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["d4cf1136-df3a-4fc2-9a21-9032949eca41"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1627-1)", "package_ndc": "72162-1627-1", "marketing_start_date": "20230516"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1627-2)", "package_ndc": "72162-1627-2", "marketing_start_date": "20230516"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-1627-3)", "package_ndc": "72162-1627-3", "marketing_start_date": "20230516"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72162-1627-4)", "package_ndc": "72162-1627-4", "marketing_start_date": "20230516"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-1627-5)", "package_ndc": "72162-1627-5", "marketing_start_date": "20230516"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-1627-7)", "package_ndc": "72162-1627-7", "marketing_start_date": "20230516"}], "brand_name": "SPIRONOLACTONE", "product_id": "72162-1627_a6caa2b8-b27e-47eb-9db8-ccfa8e8b6a8b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "72162-1627", "generic_name": "SPIRONOLACTONE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "100 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20271231"}