Package 60505-1321-5

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-1321-5
Digits Only 6050513215
Product NDC 60505-1321
Description

500 TABLET in 1 BOTTLE (60505-1321-5)

Marketing

Marketing Status
Marketed Since 2006-09-12
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"}