desmopressin acetate

Generic: desmopressin acetate

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desmopressin acetate
Generic Name desmopressin acetate
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desmopressin acetate .2 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-250
Product ID 59651-250_24866ad0-94db-46a2-96c0-b362acd0271a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213095
Listing Expiration 2026-12-31
Marketing Start 2024-03-21

Pharmacologic Class

Classes
factor viii activator [epc] increased coagulation factor viii activity [pe] increased coagulation factor viii concentration [pe] vasopressin analog [epc] vasopressins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651250
Hyphenated Format 59651-250

Supplemental Identifiers

RxCUI
833008 849515
UNII
XB13HYU18U

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 desmopressin acetate (source: ndc)
Generic Name desmopressin acetate (source: ndc)
Application Number ANDA213095 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59651-250-01)
source: ndc

Packages (1)

59651-250-01 100 TABLET in 1 BOTTLE (59651-250-01)

Ingredients (1)

desmopressin acetate (.2 mg/1)

Linked Drug Pages (1)

Desmopressin Acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24866ad0-94db-46a2-96c0-b362acd0271a", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["24866ad0-94db-46a2-96c0-b362acd0271a"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-250-01)", "package_ndc": "59651-250-01", "marketing_start_date": "20240321"}], "brand_name": "Desmopressin Acetate", "product_id": "59651-250_24866ad0-94db-46a2-96c0-b362acd0271a", "dosage_form": "TABLET", "pharm_class": ["Factor VIII Activator [EPC]", "Increased Coagulation Factor VIII Activity [PE]", "Increased Coagulation Factor VIII Concentration [PE]", "Vasopressin Analog [EPC]", "Vasopressins [CS]"], "product_ndc": "59651-250", "generic_name": "desmopressin acetate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".2 mg/1"}], "application_number": "ANDA213095", "marketing_category": "ANDA", "marketing_start_date": "20240321", "listing_expiration_date": "20261231"}