NDC 70771-1746 – Darunavir

Darunavir 800 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70771-1746

Product details

Brand name
Darunavir
Generic name
Darunavir
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214085
Marketed since
May 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Protease Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Darunavir →

Package NDC codes (3)

Package NDCDescriptionSince
70771-1746-330 TABLET, FILM COATED in 1 BOTTLE (70771-1746-3)May 1, 2024
70771-1746-5500 TABLET, FILM COATED in 1 BOTTLE (70771-1746-5)May 1, 2024
70771-1746-990 TABLET, FILM COATED in 1 BOTTLE (70771-1746-9)May 1, 2024

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