midodrine hydrochloride

Generic: midodrine hydrochloride

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midodrine hydrochloride
Generic Name midodrine hydrochloride
Labeler endo usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

midodrine hydrochloride 10 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 49884-874
Product ID 49884-874_b4a5203e-c030-4311-921d-48b17c45bc49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207169
Listing Expiration 2026-12-31
Marketing Start 2018-10-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49884874
Hyphenated Format 49884-874

Supplemental Identifiers

RxCUI
993462 993466 993470
UPC
0349884874018 0349884814014 0349884849016
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 ANDA207169 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (49884-874-01)
source: ndc

Packages (1)

49884-874-01 100 TABLET in 1 BOTTLE (49884-874-01)

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": "b4a5203e-c030-4311-921d-48b17c45bc49", "openfda": {"upc": ["0349884874018", "0349884814014", "0349884849016"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["863f12bd-d4a9-4547-8667-5dfa9e2ce6d1"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49884-874-01)", "package_ndc": "49884-874-01", "marketing_start_date": "20181029"}], "brand_name": "Midodrine Hydrochloride", "product_id": "49884-874_b4a5203e-c030-4311-921d-48b17c45bc49", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "49884-874", "generic_name": "Midodrine Hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207169", "marketing_category": "ANDA", "marketing_start_date": "20181029", "listing_expiration_date": "20261231"}