NDC 31722-838 – ABACAVIR and LAMIVUDINE

Abacavir Sulfate 600 mg/1; Lamivudine 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC31722-838

Product details

Brand name
ABACAVIR and LAMIVUDINE
Generic name
ABACAVIR and LAMIVUDINE
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205412
Marketed since
April 16, 2025
Listing expires
December 31, 2026
Pharmacologic class
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Abacavir and Lamivudine →

Package NDC codes (1)

Package NDCDescriptionSince
31722-838-301 BOTTLE in 1 CARTON (31722-838-30) / 30 TABLET, FILM COATED in 1 BOTTLEApr 16, 2025

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