Abacavir

Product NDC

70518-0559

11-digit product format

705180559

Labeler code

70518

Product ID

70518-0559_85ce41df-7425-8b2b-e053-2991aa0a40b9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Abacavir

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077844

Marketing category

ANDA

Marketing start

2017-05-30

Marketing end

0000-00-00

Substance

ABACAVIR SULFATE

Active strength

300 mg/1

Pharmacologic classes

Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record