Lamivudine and Zidovudine

Product NDC

42291-363

11-digit product format

422910363

Labeler code

42291

Product ID

42291-363_638dbc25-4869-3d56-e053-2a91aa0a9554

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lamivudine and Zidovudine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA079081

Marketing category

ANDA

Marketing start

2013-10-16

Marketing end

0000-00-00

Substance

LAMIVUDINE; ZID

Active strength

150 mg/1; mg/1

Pharmacologic classes

Hepatitis B Vir

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record