NDC 70771-1793 – Selexipag

Selexipag 200 ug/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70771-1793

Product details

Brand name
Selexipag
Generic name
Selexipag
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214302
Marketed since
February 14, 2025
Listing expires
December 31, 2026
Pharmacologic class
Prostacyclin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Selexipag →

Package NDC codes (2)

Package NDCDescriptionSince
70771-1793-6 sample60 TABLET, FILM COATED in 1 BOTTLE (70771-1793-6)Feb 14, 2025
70771-1793-8 sample140 TABLET, FILM COATED in 1 BOTTLE (70771-1793-8)Feb 14, 2025

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