desmopressin acetate
Generic: desmopressin acetate
Labeler: apotex corp.Drug Facts
Product Profile
Brand Name
desmopressin acetate
Generic Name
desmopressin acetate
Labeler
apotex corp.
Dosage Form
SPRAY
Routes
Active Ingredients
desmopressin acetate 10 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
60505-0815
Product ID
60505-0815_f90935bd-bb23-2f9c-3271-8508e92d45c4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076703
Listing Expiration
2026-12-31
Marketing Start
2020-11-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605050815
Hyphenated Format
60505-0815
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
ANDA076703 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 ug/1
Packaging
- 1 BOTTLE, SPRAY in 1 CARTON (60505-0815-0) / 50 SPRAY in 1 BOTTLE, SPRAY
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "f90935bd-bb23-2f9c-3271-8508e92d45c4", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["849506"], "spl_set_id": ["1ac423b8-27a6-4cef-4a82-c50bf81b4f49"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 CARTON (60505-0815-0) / 50 SPRAY in 1 BOTTLE, SPRAY", "package_ndc": "60505-0815-0", "marketing_start_date": "20201130"}], "brand_name": "DESMOPRESSIN ACETATE", "product_id": "60505-0815_f90935bd-bb23-2f9c-3271-8508e92d45c4", "dosage_form": "SPRAY", "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": "60505-0815", "generic_name": "DESMOPRESSIN ACETATE", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESMOPRESSIN ACETATE", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": "10 ug/1"}], "application_number": "ANDA076703", "marketing_category": "ANDA", "marketing_start_date": "20201130", "listing_expiration_date": "20261231"}