desmopressin acetate

Generic: desmopressin acetate

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desmopressin acetate
Generic Name desmopressin acetate
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desmopressin acetate .1 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-489
Product ID 23155-489_3ed8c1cf-5b26-49fc-adb2-264572e68cbe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207880
Listing Expiration 2026-12-31
Marketing Start 2017-05-26

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 23155489
Hyphenated Format 23155-489

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 ANDA207880 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-489-01)
  • 500 TABLET in 1 BOTTLE (23155-489-05)
source: ndc

Packages (2)

23155-489-01 100 TABLET in 1 BOTTLE (23155-489-01) 23155-489-05 500 TABLET in 1 BOTTLE (23155-489-05)

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": "3ed8c1cf-5b26-49fc-adb2-264572e68cbe", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["e87b6cfd-5677-4398-883d-7ced5dd678ef"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-489-01)", "package_ndc": "23155-489-01", "marketing_start_date": "20170526"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-489-05)", "package_ndc": "23155-489-05", "marketing_start_date": "20170526"}], "brand_name": "Desmopressin Acetate", "product_id": "23155-489_3ed8c1cf-5b26-49fc-adb2-264572e68cbe", "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": "23155-489", "generic_name": "Desmopressin Acetate", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".1 mg/1"}], "application_number": "ANDA207880", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}