Package 51079-453-20

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51079-453-20
Digits Only 5107945320
Product NDC 51079-453
Description

100 BLISTER PACK in 1 CARTON (51079-453-20) / 1 TABLET in 1 BLISTER PACK (51079-453-01)

Marketing

Marketing Status
Marketed Since 2006-09-11
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": "3a8743bb-679f-ae20-e063-6394a90a41c6", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993470"], "spl_set_id": ["fd28d383-add9-42a9-ad07-4d7e89f12460"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-453-20)  / 1 TABLET in 1 BLISTER PACK (51079-453-01)", "package_ndc": "51079-453-20", "marketing_start_date": "20060911"}], "brand_name": "Midodrine Hydrochloride", "product_id": "51079-453_3a8743bb-679f-ae20-e063-6394a90a41c6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "51079-453", "generic_name": "midodrine hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076577", "marketing_category": "ANDA", "marketing_start_date": "20060911", "listing_expiration_date": "20261231"}