midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler upsher-smith laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 10 mg/1

Manufacturer
Upsher-Smith laboratories, LLC

Identifiers & Regulatory

Product NDC 0245-0213
Product ID 0245-0213_18b0b9f5-6026-479e-af12-92b0e71a9d6b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076725
Listing Expiration 2026-12-31
Marketing Start 2004-11-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02450213
Hyphenated Format 0245-0213

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 ANDA076725 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0245-0213-01) / 1 TABLET in 1 BLISTER PACK (0245-0213-89)
  • 100 TABLET in 1 BOTTLE (0245-0213-11)
source: ndc

Packages (2)

0245-0213-01 100 BLISTER PACK in 1 CARTON (0245-0213-01) / 1 TABLET in 1 BLISTER PACK (0245-0213-89) 0245-0213-11 100 TABLET in 1 BOTTLE (0245-0213-11)

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": "18b0b9f5-6026-479e-af12-92b0e71a9d6b", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["4c3517f3-1c68-4ade-b5f1-c488a3a335c1"], "manufacturer_name": ["Upsher-Smith laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0245-0213-01)  / 1 TABLET in 1 BLISTER PACK (0245-0213-89)", "package_ndc": "0245-0213-01", "marketing_start_date": "20041103"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (0245-0213-11)", "package_ndc": "0245-0213-11", "marketing_start_date": "20041103"}], "brand_name": "Midodrine Hydrochloride", "product_id": "0245-0213_18b0b9f5-6026-479e-af12-92b0e71a9d6b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0245-0213", "generic_name": "midodrine hydrochloride", "labeler_name": "Upsher-Smith laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076725", "marketing_category": "ANDA", "marketing_start_date": "20041103", "listing_expiration_date": "20261231"}