Package 42708-123-30

Brand: furosemide

Generic: furosemide
NDC Package Sample

Package Facts

Identity

Package NDC 42708-123-30
Digits Only 4270812330
Product NDC 42708-123
Description

30 TABLET in 1 BOTTLE (42708-123-30)

Marketing

Marketing Status
Marketed Since 2018-05-23
Brand furosemide
Generic furosemide
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "459c0c80-5889-208c-e063-6294a90a4d0d", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["341e29d9-a6f1-4c77-ae44-9b2c423ea6b4"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-123-30)", "package_ndc": "42708-123-30", "marketing_start_date": "20180523"}], "brand_name": "Furosemide", "product_id": "42708-123_459c0c80-5889-208c-e063-6294a90a4d0d", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42708-123", "generic_name": "Furosemide", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}