# Desmopressin Acetate

NDC: 70095-026
Generic name: Desmopressin Acetate
Labeler / Manufacturer: Sun Pharmaceutical Industries Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20230403

FDA application: ANDA216922

## 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:"70095-026"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70095-026
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cdec2cc2-4fd9-474e-884f-d0599e40948f