Package 42291-561-90

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42291-561-90
Digits Only 4229156190
Product NDC 42291-561
Description

90 TABLET in 1 BOTTLE (42291-561-90)

Marketing

Marketing Status
Marketed Since 2017-05-05
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": "485ffcea-c65d-bf10-e063-6294a90a4ee1", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["1c2e8707-550f-430f-87f3-4bb3d55f4aba"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-561-90)", "package_ndc": "42291-561-90", "marketing_start_date": "20170505"}], "brand_name": "Midodrine Hydrochloride", "product_id": "42291-561_485ffcea-c65d-bf10-e063-6294a90a4ee1", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "42291-561", "generic_name": "Midodrine Hydrochloride", "labeler_name": "AvKARE", "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": "20170505", "listing_expiration_date": "20271231"}