LUNESTA
Identification of Lunesta
No description |
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Active ingredient
eszopiclone, 1 MG
DIN: 02453207
Dosage form(s): TABLET
Route(s) of administration: ORAL
Schedule: Prescription
Company: SUMITOMO PHARMA CANADA, INC.
Date: 30-AUG-2024
ATC:
- N05 — PSYCHOLEPTICS (ATC, ATC/DDD, )
- N05C — HYPNOTICS AND SEDATIVES (ATC, ATC/DDD)
- N05CF — Benzodiazepine related drugs (ATC, ATC/DDD)
- N05CF04 — ESZOPICLONE (ATC/DDD)
Pharmaceutical standard: USP