# Desmopressin Acetate

NDC: 70095-031
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: 20230620

FDA application: ANDA216904

## 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:"70095-031"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70095-031
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=539d7da2-72b8-45f9-836c-4e3351dd488e