ZERIT

Product NDC

0003-1968

11-digit product format

000031968

Labeler code

0003

Product ID

0003-1968_38a2d755-5358-43e3-b005-ab103e97789b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

stavudine

Dosage form

POWDER, FOR SOLUTION

Route

ORAL

Labeler

E.R. Squibb & Sons, L.L.C.

Application

NDA020413

Marketing category

NDA

Marketing start

2017-06-13

Marketing end

0000-00-00

Substance

STAVUDINE

Active strength

1 mg/mL

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

2019-12-31

Current FDA listing

Historical FDA.report record