NDC 65862-335 – Abacavir and Lamivudine

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

Human Prescription Drug

Product NDC65862-335

Product details

Brand name
Abacavir and Lamivudine
Generic name
Abacavir and Lamivudine
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090159
Marketed since
November 15, 2018
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 (2)

Package NDCDescriptionSince
65862-335-1010 BLISTER PACK in 1 CARTON (65862-335-10) / 10 TABLET, FILM COATED in 1 BLISTER PACKNov 15, 2018
65862-335-301 BOTTLE in 1 CARTON (65862-335-30) / 30 TABLET, FILM COATED in 1 BOTTLENov 15, 2018

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