midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-905
Product ID 71205-905_fac1a712-e714-4137-8604-2ba0f048901c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207849
Listing Expiration 2026-12-31
Marketing Start 2020-10-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205905
Hyphenated Format 71205-905

Supplemental Identifiers

RxCUI
993462 993466 993470
UPC
0371205906306 0371205905309 0371205904302
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 ANDA207849 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (71205-905-00)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (71205-905-11)
  • 30 TABLET in 1 BOTTLE, PLASTIC (71205-905-30)
  • 500 TABLET in 1 BOTTLE, PLASTIC (71205-905-55)
  • 60 TABLET in 1 BOTTLE, PLASTIC (71205-905-60)
  • 120 TABLET in 1 BOTTLE, PLASTIC (71205-905-72)
  • 90 TABLET in 1 BOTTLE, PLASTIC (71205-905-90)
source: ndc

Packages (7)

71205-905-00 100 TABLET in 1 BOTTLE, PLASTIC (71205-905-00) 71205-905-11 1000 TABLET in 1 BOTTLE, PLASTIC (71205-905-11) 71205-905-30 30 TABLET in 1 BOTTLE, PLASTIC (71205-905-30) 71205-905-55 500 TABLET in 1 BOTTLE, PLASTIC (71205-905-55) 71205-905-60 60 TABLET in 1 BOTTLE, PLASTIC (71205-905-60) 71205-905-72 120 TABLET in 1 BOTTLE, PLASTIC (71205-905-72) 71205-905-90 90 TABLET in 1 BOTTLE, PLASTIC (71205-905-90)

Ingredients (1)

midodrine hydrochloride (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": "fac1a712-e714-4137-8604-2ba0f048901c", "openfda": {"upc": ["0371205906306", "0371205905309", "0371205904302"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["0aebf5f9-8cfa-4b77-ba40-821ce0a2b266"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (71205-905-00)", "package_ndc": "71205-905-00", "marketing_start_date": "20210720"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (71205-905-11)", "package_ndc": "71205-905-11", "marketing_start_date": "20210720"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71205-905-30)", "package_ndc": "71205-905-30", "marketing_start_date": "20210720"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (71205-905-55)", "package_ndc": "71205-905-55", "marketing_start_date": "20210720"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71205-905-60)", "package_ndc": "71205-905-60", "marketing_start_date": "20210720"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (71205-905-72)", "package_ndc": "71205-905-72", "marketing_start_date": "20210720"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71205-905-90)", "package_ndc": "71205-905-90", "marketing_start_date": "20210720"}], "brand_name": "Midodrine Hydrochloride", "product_id": "71205-905_fac1a712-e714-4137-8604-2ba0f048901c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "71205-905", "generic_name": "midodrine hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA207849", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}