Package 63629-1120-1

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 63629-1120-1
Digits Only 6362911201
Product NDC 63629-1120
Description

500 TABLET in 1 BOTTLE, PLASTIC (63629-1120-1)

Marketing

Marketing Status
Marketed Since 2020-07-30
Brand furosemide
Generic furosemide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "620c9a96-bc8b-4966-ab6d-3a77ecb29747", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732"], "spl_set_id": ["01a5f094-b473-4e46-9e61-69d5ec6dd766"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (63629-1120-1)", "package_ndc": "63629-1120-1", "marketing_start_date": "20200730"}], "brand_name": "Furosemide", "product_id": "63629-1120_620c9a96-bc8b-4966-ab6d-3a77ecb29747", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "63629-1120", "generic_name": "furosemide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20200730", "listing_expiration_date": "20261231"}