midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: novugen pharma (usa) llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler novugen pharma (usa) llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 2.5 mg/1

Manufacturer
Novugen Pharma (USA) LLC

Identifiers & Regulatory

Product NDC 82293-003
Product ID 82293-003_451b5336-7460-7ffc-e063-6294a90aa15b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211973
Listing Expiration 2026-12-31
Marketing Start 2023-10-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82293003
Hyphenated Format 82293-003

Supplemental Identifiers

RxCUI
993462 993466 993470
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 ANDA211973 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82293-003-10)
source: ndc

Packages (1)

82293-003-10 100 TABLET in 1 BOTTLE (82293-003-10)

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": "451b5336-7460-7ffc-e063-6294a90aa15b", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["2bf011fe-d114-42a4-93e2-76a993a3ba34"], "manufacturer_name": ["Novugen Pharma (USA) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82293-003-10)", "package_ndc": "82293-003-10", "marketing_start_date": "20231018"}], "brand_name": "Midodrine Hydrochloride", "product_id": "82293-003_451b5336-7460-7ffc-e063-6294a90aa15b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "82293-003", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Novugen Pharma (USA) LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA211973", "marketing_category": "ANDA", "marketing_start_date": "20231018", "listing_expiration_date": "20261231"}