NDC 31722-535 – Tenofovir Disoproxil Fumarate

Tenofovir Disoproxil Fumarate 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC31722-535

Product details

Brand name
Tenofovir Disoproxil Fumarate
Generic name
Tenofovir Disoproxil Fumarate
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090636
Marketed since
January 26, 2018
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 Tenofovir Disoproxil Fumarate →

Package NDC codes (5)

Package NDCDescriptionSince
31722-535-01100 TABLET, FILM COATED in 1 BOTTLE (31722-535-01)Jan 26, 2018
31722-535-05500 TABLET, FILM COATED in 1 BOTTLE (31722-535-05)Jan 26, 2018
31722-535-101000 TABLET, FILM COATED in 1 BOTTLE (31722-535-10)Jan 26, 2018
31722-535-3030 TABLET, FILM COATED in 1 BOTTLE (31722-535-30)Jan 26, 2018
31722-535-6060 TABLET, FILM COATED in 1 BOTTLE (31722-535-60)Jan 26, 2018

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