midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 2.5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-465
Product ID 72789-465_3e13fe26-c4c4-17ce-e063-6394a90ae0bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212543
Listing Expiration 2026-12-31
Marketing Start 2019-08-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789465
Hyphenated Format 72789-465

Supplemental Identifiers

RxCUI
993466
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 ANDA212543 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-465-01)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-465-90)
source: ndc

Packages (2)

72789-465-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-465-01) 72789-465-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-465-90)

Ingredients (1)

midodrine hydrochloride (2.5 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": "3e13fe26-c4c4-17ce-e063-6394a90ae0bd", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993466"], "spl_set_id": ["54ded041-c78c-4646-a1cc-c94afcd62690"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-465-01)", "package_ndc": "72789-465-01", "marketing_start_date": "20241226"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-465-90)", "package_ndc": "72789-465-90", "marketing_start_date": "20250905"}], "brand_name": "Midodrine Hydrochloride", "product_id": "72789-465_3e13fe26-c4c4-17ce-e063-6394a90ae0bd", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "72789-465", "generic_name": "Midodrine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA212543", "marketing_category": "ANDA", "marketing_start_date": "20190819", "listing_expiration_date": "20261231"}