NDC 42385-962 – Abacavir and Lamivudine

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

Human Prescription Drug

Product NDC42385-962

Product details

Brand name
Abacavir and Lamivudine
Generic name
Abacavir and Lamivudine
Labeler
Laurus Labs Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216332
Marketed since
July 25, 2022
Listing expires
December 31, 2027
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 (3)

Package NDCDescriptionSince
42385-962-18180 TABLET, FILM COATED in 1 BOTTLE (42385-962-18)Jul 25, 2022
42385-962-3030 TABLET, FILM COATED in 1 BOTTLE (42385-962-30)Jul 25, 2022
42385-962-9090 TABLET, FILM COATED in 1 BOTTLE (42385-962-90)Jul 25, 2022

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