desmopressin acetate

Generic: desmopressin acetate

Labeler: nordic pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name desmopressin acetate
Generic Name desmopressin acetate
Labeler nordic pharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desmopressin acetate .2 mg/1

Manufacturer
Nordic Pharma, Inc.

Identifiers & Regulatory

Product NDC 69918-201
Product ID 69918-201_8f843a4f-10ba-4f8c-a86e-f599dbb7f322
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019955
Listing Expiration 2026-12-31
Marketing Start 2015-12-10

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 69918201
Hyphenated Format 69918-201

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 NDA019955 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .2 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (69918-201-01) / 100 TABLET in 1 BOTTLE
source: ndc

Packages (1)

69918-201-01 1 BOTTLE in 1 CARTON (69918-201-01) / 100 TABLET in 1 BOTTLE

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": "8f843a4f-10ba-4f8c-a86e-f599dbb7f322", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["c01048e8-d28f-4085-9c37-3d5d48395a77"], "manufacturer_name": ["Nordic Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69918-201-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "69918-201-01", "marketing_start_date": "20151210"}], "brand_name": "Desmopressin Acetate", "product_id": "69918-201_8f843a4f-10ba-4f8c-a86e-f599dbb7f322", "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": "69918-201", "generic_name": "Desmopressin Acetate", "labeler_name": "Nordic Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".2 mg/1"}], "application_number": "NDA019955", "marketing_category": "NDA", "marketing_start_date": "20151210", "listing_expiration_date": "20261231"}