Package 70756-010-11

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70756-010-11
Digits Only 7075601011
Product NDC 70756-010
Description

100 TABLET in 1 BOTTLE (70756-010-11)

Marketing

Marketing Status
Marketed Since 2023-11-01
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": "e8d87cc3-32ad-45ec-9e23-9e15d92e66b5", "openfda": {"upc": ["0370756049111", "0370756010111"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["99d4aa03-81f7-4b43-a7b4-4ecc5ad13304"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70756-010-11)", "package_ndc": "70756-010-11", "marketing_start_date": "20231101"}], "brand_name": "Midodrine Hydrochloride", "product_id": "70756-010_e8d87cc3-32ad-45ec-9e23-9e15d92e66b5", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "70756-010", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA217271", "marketing_category": "ANDA", "marketing_start_date": "20231101", "listing_expiration_date": "20261231"}