NDC 72319-025 – Maraviroc

Maraviroc 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72319-025

Product details

Brand name
Maraviroc
Generic name
Maraviroc
Labeler
i3 Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217114
Marketed since
September 15, 2023
Listing expires
December 31, 2026
Pharmacologic class
CCR5 Co-receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Maraviroc →

Package NDC codes (1)

Package NDCDescriptionSince
72319-025-0260 TABLET, FILM COATED in 1 BOTTLE (72319-025-02)Sep 15, 2023

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