NDC 33342-440 – Abacavir and Lamivudine

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

Human Prescription Drug

Product NDC33342-440

Product details

Brand name
Abacavir and Lamivudine
Generic name
Abacavir and Lamivudine
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212663
Marketed since
December 20, 2024
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 (3)

Package NDCDescriptionSince
33342-440-0730 TABLET, FILM COATED in 1 BOTTLE (33342-440-07)Dec 20, 2024
33342-440-145 BLISTER PACK in 1 CARTON (33342-440-14) / 6 TABLET, FILM COATED in 1 BLISTER PACK (33342-440-02)Dec 20, 2024
33342-440-9810 BLISTER PACK in 1 CARTON (33342-440-98) / 6 TABLET, FILM COATED in 1 BLISTER PACK (33342-440-02)Dec 20, 2024

Other Abacavir and Lamivudine products