DailyMed label

Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride

DailyMed label · Sagent Pharmaceuticals · version 2

Key facts

Product Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride
Labeler Sagent Pharmaceuticals
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients dexmedetomidine hydrochloride
Active ingredient UNIIs 1018WH7F9I
Application number 217308
Route INTRAVENOUS
NDC package codes 25021-615-50, 25021-615-51
Effective date Oct 6, 2023
Set ID a99335d0-1e87-4180-bde3-cbb12bf91a52

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • None Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

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