midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 10 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-563
Product ID 50268-563_32fa2977-8701-5efb-e063-6394a90a2dff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077746
Listing Expiration 2026-12-31
Marketing Start 2019-08-26

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268563
Hyphenated Format 50268-563

Supplemental Identifiers

RxCUI
993462 993466 993470
UNII
59JV96YTXV

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name midodrine hydrochloride (source: ndc)
Generic Name midodrine hydrochloride (source: ndc)
Application Number ANDA077746 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 50 TABLET in 1 BOX (50268-563-15)
source: ndc

Packages (1)

50268-563-15 50 TABLET in 1 BOX (50268-563-15)

Ingredients (1)

midodrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Midodrine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "32fa2977-8701-5efb-e063-6394a90a2dff", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["9106776e-601a-4e3c-e053-2995a90a5435"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOX (50268-563-15)", "package_ndc": "50268-563-15", "marketing_start_date": "20190826"}], "brand_name": "Midodrine Hydrochloride", "product_id": "50268-563_32fa2977-8701-5efb-e063-6394a90a2dff", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "50268-563", "generic_name": "Midodrine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077746", "marketing_category": "ANDA", "marketing_start_date": "20190826", "listing_expiration_date": "20261231"}