midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 2.5 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6817
Product ID 0904-6817_ead857d5-e960-4309-83f4-d9537cd32b9f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077746
Listing Expiration 2026-12-31
Marketing Start 2006-09-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046817
Hyphenated Format 0904-6817

Supplemental Identifiers

RxCUI
993462 993466 993470
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 ANDA077746 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 CARTON (0904-6817-06) / 1 TABLET in 1 BLISTER PACK
  • 100 BLISTER PACK in 1 CARTON (0904-6817-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

0904-6817-06 50 BLISTER PACK in 1 CARTON (0904-6817-06) / 1 TABLET in 1 BLISTER PACK 0904-6817-61 100 BLISTER PACK in 1 CARTON (0904-6817-61) / 1 TABLET in 1 BLISTER PACK

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": "ead857d5-e960-4309-83f4-d9537cd32b9f", "openfda": {"unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["164dce3b-1927-497e-884a-a2c72958beb9"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6817-06)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6817-06", "marketing_start_date": "20060912"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6817-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6817-61", "marketing_start_date": "20060912"}], "brand_name": "Midodrine Hydrochloride", "product_id": "0904-6817_ead857d5-e960-4309-83f4-d9537cd32b9f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0904-6817", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA077746", "marketing_category": "ANDA", "marketing_start_date": "20060912", "listing_expiration_date": "20261231"}