Abacavir Sulfate

Product NDC

70518-0640

11-digit product format

705180640

Labeler code

70518

Product ID

70518-0640_883e9716-e265-25dc-e053-2a95a90a4cf0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Abacavir Sulfate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA201570

Marketing category

ANDA

Marketing start

2017-07-26

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