Package 42708-126-30
Brand: spironolactone
Generic: spironolactonePackage Facts
Identity
Package NDC
42708-126-30
Digits Only
4270812630
Product NDC
42708-126
Description
30 TABLET in 1 BOTTLE (42708-126-30)
Marketing
Marketing Status
Brand
spironolactone
Generic
spironolactone
Sample Package
Yes
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459c0193-3a84-878d-e063-6294a90afc31", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["eb314e91-6dd5-4bdb-af35-5d147b20339c"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-126-30)", "package_ndc": "42708-126-30", "marketing_start_date": "20180523"}], "brand_name": "Spironolactone", "product_id": "42708-126_459c0193-3a84-878d-e063-6294a90afc31", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "42708-126", "generic_name": "Spironolactone", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA091426", "marketing_category": "ANDA", "marketing_start_date": "20100802", "listing_expiration_date": "20261231"}