Package 68071-1809-1

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 68071-1809-1
Digits Only 6807118091
Product NDC 68071-1809
Product ID 68071-1809_1d51781e-6c38-d57f-e063-6294a90a5ce2
Description

100 TABLET in 1 BOTTLE (68071-1809-1)

Marketing

Marketing Status
Marketed Since 2019-01-29
Brand furosemide
Generic furosemide
Sample Package No

Linked Drug Pages (1)

Furosemide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d51781e-6c38-d57f-e063-6294a90a5ce2", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["809b4f68-4fca-c201-e053-2a91aa0ac18e"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-1809-1)", "package_ndc": "68071-1809-1", "marketing_start_date": "20190129"}], "brand_name": "Furosemide", "product_id": "68071-1809_1d51781e-6c38-d57f-e063-6294a90a5ce2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "68071-1809", "generic_name": "Furosemide", "labeler_name": "NuCare Pharmaceuticals,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"}