NDC 31722-752 – Lamivudine

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

Human Prescription Drug

Product NDC31722-752

Product details

Brand name
Lamivudine
Generic name
Lamivudine
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203260
Marketed since
January 2, 2014
Listing expires
December 31, 2027
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 (4)

Package NDCDescriptionSince
31722-752-06600 TABLET, FILM COATED in 1 BOTTLE (31722-752-06)Jan 2, 2014
31722-752-3110 TABLET, FILM COATED in 1 BLISTER PACK (31722-752-31)Jan 2, 2014
31722-752-32100 TABLET, FILM COATED in 1 CARTON (31722-752-32)Jan 2, 2014
31722-752-6060 TABLET, FILM COATED in 1 BOTTLE (31722-752-60)Jan 2, 2014

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