Package 49884-814-01

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49884-814-01
Digits Only 4988481401
Product NDC 49884-814
Product ID 49884-814_b4a5203e-c030-4311-921d-48b17c45bc49
Description

100 TABLET in 1 BOTTLE (49884-814-01)

Marketing

Marketing Status
Marketed Since 2018-10-29
Brand midodrine hydrochloride
Generic midodrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Midodrine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b4a5203e-c030-4311-921d-48b17c45bc49", "openfda": {"upc": ["0349884874018", "0349884814014", "0349884849016"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["863f12bd-d4a9-4547-8667-5dfa9e2ce6d1"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49884-814-01)", "package_ndc": "49884-814-01", "marketing_start_date": "20181029"}], "brand_name": "Midodrine Hydrochloride", "product_id": "49884-814_b4a5203e-c030-4311-921d-48b17c45bc49", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "49884-814", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA207169", "marketing_category": "ANDA", "marketing_start_date": "20181029", "listing_expiration_date": "20261231"}