Package 60505-1321-1
Brand: midodrine hydrochloride
Generic: midodrine hydrochloridePackage Facts
Identity
Package NDC
60505-1321-1
Digits Only
6050513211
Product NDC
60505-1321
Description
100 TABLET in 1 BOTTLE (60505-1321-1)
Marketing
Marketing Status
Brand
midodrine hydrochloride
Generic
midodrine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef40d4d7-e3ab-70fd-f7a0-b9c02055f734", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["aec0d2de-ce83-b7c2-5d10-740607d50521"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-1321-1)", "package_ndc": "60505-1321-1", "marketing_start_date": "20060912"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (60505-1321-3)", "package_ndc": "60505-1321-3", "marketing_start_date": "20060912"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (60505-1321-5)", "package_ndc": "60505-1321-5", "marketing_start_date": "20060912"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (60505-1321-8)", "package_ndc": "60505-1321-8", "marketing_start_date": "20060912"}], "brand_name": "Midodrine Hydrochloride", "product_id": "60505-1321_ef40d4d7-e3ab-70fd-f7a0-b9c02055f734", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "60505-1321", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077746", "marketing_category": "ANDA", "marketing_start_date": "20060912", "listing_expiration_date": "20261231"}