Package 0904-7178-61
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
0904-7178-61
Digits Only
0904717861
Product NDC
0904-7178
Description
100 BLISTER PACK in 1 CARTON (0904-7178-61) / 1 TABLET in 1 BLISTER PACK
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": "519435a0-5141-403d-8642-f6fe3006c8bc", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429", "313988"], "spl_set_id": ["6be1addd-a811-47fc-8650-6870d661c234"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7178-61) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7178-61", "marketing_start_date": "20040326"}], "brand_name": "Furosemide", "product_id": "0904-7178_519435a0-5141-403d-8642-f6fe3006c8bc", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0904-7178", "generic_name": "furosemide", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}