United States · FDA National Drug Code directory

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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
71390-011_4da618a9-2e04-4d75-922b-173d22b4e84c
Product NDC
71390-011
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
remimazolam besylate
Labeler
Acacia Pharma, Ltd.
Marketing category
NDA
Marketing start / end (source format)
20201006
Source listing expiry
20261231

Source-listed ingredients

  • REMIMAZOLAM BESYLATE — 2.5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 VIAL in 1 CARTON (71390-011-11) / 8 mL in 1 VIAL (71390-011-00) · 71390-011-11

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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