NDC 59651-104 – Eletriptan Hydrobromide

Eletriptan Hydrobromide 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC59651-104

Product details

Brand name
Eletriptan Hydrobromide
Generic name
Eletriptan Hydrobromide
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210708
Marketed since
January 15, 2019
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Eletriptan hydrobromide →

Package NDC codes (1)

Package NDCDescriptionSince
59651-104-691 BLISTER PACK in 1 CARTON (59651-104-69) / 6 TABLET, FILM COATED in 1 BLISTER PACK (59651-104-06)Jan 15, 2019

Recalls mentioning this NDC

Other Eletriptan hydrobromide products