SPIRONOLACTONE

Generic: SPIRONOLACTONE

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name SPIRONOLACTONE
Generic Name SPIRONOLACTONE
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

SPIRONOLACTONE 25 mg/1

Identifiers & Regulatory

Product NDC 70518-3118
Product ID 70518-3118_3a1f895d-f849-446e-e063-6394a90a098d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089424
Listing Expiration 2026-12-31
Marketing Start 2021-06-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183118
Hyphenated Format 70518-3118

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (70518-3118-2)
source: ndc

Packages (1)

70518-3118-2 100 TABLET in 1 BOTTLE, PLASTIC (70518-3118-2)

Ingredients (1)

SPIRONOLACTONE (25 mg/1)

Linked Drug Pages (1)

SPIRONOLACTONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a1f895d-f849-446e-e063-6394a90a098d", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["093f2eb9-7c3b-4960-98cc-30d3d90aa094"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-3118-2)", "package_ndc": "70518-3118-2", "marketing_start_date": "20230830"}], "brand_name": "SPIRONOLACTONE", "product_id": "70518-3118_3a1f895d-f849-446e-e063-6394a90a098d", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "70518-3118", "generic_name": "SPIRONOLACTONE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "20210610", "listing_expiration_date": "20261231"}