midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler northstar rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 10 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 72603-607
Product ID 72603-607_3370f087-6bac-2032-e063-6394a90a9a60
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212543
Listing Expiration 2026-12-31
Marketing Start 2025-04-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603607
Hyphenated Format 72603-607

Supplemental Identifiers

RxCUI
993462 993466 993470
UPC
0372603606010 0372603605013 0372603607017
UNII
59JV96YTXV

Packaging Origin

Original Packager
true

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 ANDA212543 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72603-607-01)
source: ndc

Packages (1)

72603-607-01 100 TABLET in 1 BOTTLE (72603-607-01)

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": "3370f087-6bac-2032-e063-6394a90a9a60", "openfda": {"upc": ["0372603606010", "0372603605013", "0372603607017"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["b015c98f-57e6-410b-9c9d-8898aa22082a"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-607-01)", "package_ndc": "72603-607-01", "marketing_start_date": "20250421"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72603-607_3370f087-6bac-2032-e063-6394a90a9a60", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72603-607", "generic_name": "Midodrine Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA212543", "marketing_category": "ANDA", "marketing_start_date": "20250421", "listing_expiration_date": "20261231"}