United States · FDA National Drug Code directory
Desmopressin Acetate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70095-031_2a4f6931-2711-4831-8096-7acb266f4e22
- Product NDC
- 70095-031
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Desmopressin Acetate
- Labeler
- Sun Pharmaceutical Industries Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230620
- Source listing expiry
- 20261231
Source-listed ingredients
- DESMOPRESSIN ACETATE — 4 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (70095-031-01) / 10 mL in 1 VIAL · 70095-031-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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