NDC 72865-232 – Maraviroc

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

Human Prescription Drug

Product NDC72865-232

Product details

Brand name
Maraviroc
Generic name
Maraviroc
Labeler
XLCare Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203347
Marketed since
June 1, 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
72865-232-6060 TABLET, FILM COATED in 1 BOTTLE (72865-232-60)Jun 1, 2023

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