desmopressin acetate

Generic: desmopressin acetate

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desmopressin acetate
Generic Name desmopressin acetate
Labeler apotex corp.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desmopressin acetate .1 mg/1

Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-0257
Product ID 60505-0257_41d13d8f-eeae-838d-fd10-bf7f568e903b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077414
Listing Expiration 2026-12-31
Marketing Start 2006-03-07

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 605050257
Hyphenated Format 60505-0257

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 ANDA077414 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (60505-0257-1)
source: ndc

Packages (1)

60505-0257-1 100 TABLET in 1 BOTTLE (60505-0257-1)

Ingredients (1)

desmopressin acetate (.1 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": "41d13d8f-eeae-838d-fd10-bf7f568e903b", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["72aeef35-c102-b628-0219-9822651887eb"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-0257-1)", "package_ndc": "60505-0257-1", "marketing_start_date": "20060307"}], "brand_name": "Desmopressin Acetate", "product_id": "60505-0257_41d13d8f-eeae-838d-fd10-bf7f568e903b", "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": "60505-0257", "generic_name": "desmopressin acetate", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".1 mg/1"}], "application_number": "ANDA077414", "marketing_category": "ANDA", "marketing_start_date": "20060307", "listing_expiration_date": "20261231"}