midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 10 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-435
Product ID 64980-435_311a8e3c-0112-4c91-a7cc-92709b41f170
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207613
Listing Expiration 2026-12-31
Marketing Start 2019-04-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64980435
Hyphenated Format 64980-435

Supplemental Identifiers

RxCUI
993462 993466 993470
UPC
0364980435017 0364980433013 0364980434010
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 ANDA207613 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (64980-435-01)
source: ndc

Packages (1)

64980-435-01 100 TABLET in 1 BOTTLE (64980-435-01)

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": "311a8e3c-0112-4c91-a7cc-92709b41f170", "openfda": {"upc": ["0364980435017", "0364980433013", "0364980434010"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["ffd4dfb9-a6d8-4c81-8b8c-8228d9e2f93e"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64980-435-01)", "package_ndc": "64980-435-01", "marketing_start_date": "20190401"}], "brand_name": "Midodrine Hydrochloride", "product_id": "64980-435_311a8e3c-0112-4c91-a7cc-92709b41f170", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "64980-435", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207613", "marketing_category": "ANDA", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}