Package 67046-1512-3

Brand: midodrine hydrochloride

Generic: midodrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1512-3
Digits Only 6704615123
Product NDC 67046-1512
Product ID 67046-1512_2d1b581e-1683-9af6-e063-6394a90ac136
Description

30 TABLET in 1 BLISTER PACK (67046-1512-3)

Marketing

Marketing Status
Marketed Since 2025-02-01
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": "2d1b581e-1683-9af6-e063-6394a90ac136", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993470"], "spl_set_id": ["2d1b58a7-ec7f-f3ea-e063-6294a90a27fb"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1512-3)", "package_ndc": "67046-1512-3", "marketing_start_date": "20250201"}], "brand_name": "Midodrine Hydrochloride", "product_id": "67046-1512_2d1b581e-1683-9af6-e063-6394a90ac136", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "67046-1512", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA217271", "marketing_category": "ANDA", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}