NDC 31722-001 – Lamivudine

Lamivudine 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC31722-001

Product details

Brand name
Lamivudine
Generic name
Lamivudine
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211306
Marketed since
March 21, 2019
Listing expires
December 31, 2026
Pharmacologic class
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lamivudine →

Package NDC codes (2)

Package NDCDescriptionSince
31722-001-0220 BLISTER PACK in 1 CARTON (31722-001-02) / 10 TABLET, FILM COATED in 1 BLISTER PACKMar 21, 2019
31722-001-6060 TABLET, FILM COATED in 1 BOTTLE (31722-001-60)Mar 21, 2019

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