desmopressin acetate

Generic: desmopressin acetate

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desmopressin acetate
Generic Name desmopressin acetate
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desmopressin acetate .2 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-461
Product ID 51655-461_490efdbc-280a-2644-e063-6294a90a583d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210371
Listing Expiration 2027-12-31
Marketing Start 2020-10-29

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 51655461
Hyphenated Format 51655-461

Supplemental Identifiers

RxCUI
833008
UNII
XB13HYU18U

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 ANDA210371 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-461-52)
source: ndc

Packages (1)

51655-461-52 30 TABLET in 1 BOTTLE, PLASTIC (51655-461-52)

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": "490efdbc-280a-2644-e063-6294a90a583d", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008"], "spl_set_id": ["f306e2d4-781f-ff8f-e053-2a95a90ad15b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-461-52)", "package_ndc": "51655-461-52", "marketing_start_date": "20201029"}], "brand_name": "Desmopressin Acetate", "product_id": "51655-461_490efdbc-280a-2644-e063-6294a90a583d", "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": "51655-461", "generic_name": "Desmopressin Acetate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".2 mg/1"}], "application_number": "ANDA210371", "marketing_category": "ANDA", "marketing_start_date": "20201029", "listing_expiration_date": "20271231"}