desmopressin acetate
Generic: desmopressin acetate
Labeler: nordic pharma, inc.Drug Facts
Product Profile
Brand Name
desmopressin acetate
Generic Name
desmopressin acetate
Labeler
nordic pharma, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
desmopressin acetate 4 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
69918-901
Product ID
69918-901_13ec577b-9bd8-4429-ad53-f8bf5a118995
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018938
Listing Expiration
2026-12-31
Marketing Start
2016-01-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69918901
Hyphenated Format
69918-901
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
NDA018938 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 ug/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (69918-901-10) / 10 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (3)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "13ec577b-9bd8-4429-ad53-f8bf5a118995", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["849501", "1723232"], "spl_set_id": ["29df0492-f7ef-47bb-aa67-4ef9e5c2846f"], "manufacturer_name": ["Nordic Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (69918-901-10) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "69918-901-10", "marketing_start_date": "20160120"}], "brand_name": "Desmopressin Acetate", "product_id": "69918-901_13ec577b-9bd8-4429-ad53-f8bf5a118995", "dosage_form": "SOLUTION", "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": "69918-901", "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": "4 ug/mL"}], "application_number": "NDA018938", "marketing_category": "NDA", "marketing_start_date": "20160120", "listing_expiration_date": "20261231"}