# Desmopressin acetate

NDC: 71288-441
Generic name: Desmopressin acetate
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20260213

FDA application: ANDA074888

## Active ingredients

- DESMOPRESSIN ACETATE: 4 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-441"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-441
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2a2a6eba-c5bf-4ee4-bb18-c992ae59dce5