desmopressin acetate

Generic: desmopressin acetate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desmopressin acetate
Generic Name desmopressin acetate
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

desmopressin acetate .1 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-721
Product ID 60687-721_437dc780-8fd1-6205-e063-6394a90a19db
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077414
Listing Expiration 2026-12-31
Marketing Start 2024-02-16

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 60687721
Hyphenated Format 60687-721

Supplemental Identifiers

RxCUI
833008 849515
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 ANDA077414 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-721-21) / 1 TABLET in 1 BLISTER PACK (60687-721-11)
source: ndc

Packages (1)

60687-721-21 30 BLISTER PACK in 1 CARTON (60687-721-21) / 1 TABLET in 1 BLISTER PACK (60687-721-11)

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": "437dc780-8fd1-6205-e063-6394a90a19db", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["833008", "849515"], "spl_set_id": ["0d447b48-3f4b-430e-9e68-d8b9401c002e"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-721-21)  / 1 TABLET in 1 BLISTER PACK (60687-721-11)", "package_ndc": "60687-721-21", "marketing_start_date": "20240216"}], "brand_name": "Desmopressin Acetate", "product_id": "60687-721_437dc780-8fd1-6205-e063-6394a90a19db", "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": "60687-721", "generic_name": "desmopressin acetate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desmopressin Acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": ".1 mg/1"}], "application_number": "ANDA077414", "marketing_category": "ANDA", "marketing_start_date": "20240216", "listing_expiration_date": "20261231"}