Package 30698-067-10

Brand: lasix

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 30698-067-10
Digits Only 3069806710
Product NDC 30698-067
Description

1000 TABLET in 1 BOTTLE (30698-067-10)

Marketing

Marketing Status
Marketed Since 1978-04-24
Brand lasix
Generic furosemide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4002943d-0b4b-4ff0-e063-6394a90ae63b", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0330698060018", "0330698066058", "0330698067017"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "200801", "200809", "205732", "310429", "313988"], "spl_set_id": ["2c9b4d8f-0770-482d-a9e6-9c616a440b1a"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-067-01)", "package_ndc": "30698-067-01", "marketing_start_date": "19780424"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (30698-067-10)", "package_ndc": "30698-067-10", "marketing_start_date": "19780424"}], "brand_name": "Lasix", "product_id": "30698-067_4002943d-0b4b-4ff0-e063-6394a90ae63b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "30698-067", "generic_name": "FUROSEMIDE", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lasix", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "NDA016273", "marketing_category": "NDA", "marketing_start_date": "19780424", "listing_expiration_date": "20261231"}