Package 67296-2136-3
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
67296-2136-3
Digits Only
6729621363
Product NDC
67296-2136
Description
30 TABLET in 1 BOTTLE (67296-2136-3)
Marketing
Marketing Status
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": "46aca8aa-d9cd-f44a-e063-6294a90aef3e", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0364980564014"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["37457273-38a1-f938-e063-6294a90a50ab"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2136-3)", "package_ndc": "67296-2136-3", "marketing_start_date": "20221105"}], "brand_name": "Furosemide", "product_id": "67296-2136_46aca8aa-d9cd-f44a-e063-6294a90aef3e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "67296-2136", "generic_name": "Furosemide", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA216629", "marketing_category": "ANDA", "marketing_start_date": "20221105", "listing_expiration_date": "20261231"}