Package 63629-1214-1
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
63629-1214-1
Digits Only
6362912141
Product NDC
63629-1214
Description
1000 TABLET in 1 BOTTLE (63629-1214-1)
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": "ddf690b2-6661-4f06-af84-322d335fa74b", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["3ad12e70-3c2e-44af-bb6b-5762d181c76b"], "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": "1000 TABLET in 1 BOTTLE (63629-1214-1)", "package_ndc": "63629-1214-1", "marketing_start_date": "20210114"}], "brand_name": "Furosemide", "product_id": "63629-1214_ddf690b2-6661-4f06-af84-322d335fa74b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "63629-1214", "generic_name": "furosemide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}