desmopressin acetate

Generic: desmopressin acetate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desmopressin acetate
Generic Name desmopressin acetate
Labeler sun pharmaceutical industries, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

desmopressin acetate 4 ug/mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-529
Product ID 62756-529_129770b0-b59a-4ee3-bc07-2168544c1424
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091280
Listing Expiration 2026-12-31
Marketing Start 2014-02-20

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 62756529
Hyphenated Format 62756-529

Supplemental Identifiers

RxCUI
849501
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 ANDA091280 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 4 ug/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 CARTON (62756-529-26) / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

62756-529-26 1 VIAL, MULTI-DOSE in 1 CARTON (62756-529-26) / 10 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

desmopressin acetate (4 ug/mL)

Linked Drug Pages (2)

desmopressin acetate ndc-match (0.9) Desmopressin Acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "129770b0-b59a-4ee3-bc07-2168544c1424", "openfda": {"unii": ["XB13HYU18U"], "rxcui": ["849501"], "spl_set_id": ["2dc2cec8-6953-4a33-9356-11534fba1fb8"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (62756-529-26)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "62756-529-26", "marketing_start_date": "20140220"}], "brand_name": "desmopressin acetate", "product_id": "62756-529_129770b0-b59a-4ee3-bc07-2168544c1424", "dosage_form": "INJECTION, 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": "62756-529", "generic_name": "desmopressin acetate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "desmopressin acetate", "active_ingredients": [{"name": "DESMOPRESSIN ACETATE", "strength": "4 ug/mL"}], "application_number": "ANDA091280", "marketing_category": "ANDA", "marketing_start_date": "20140220", "listing_expiration_date": "20261231"}