Ribavirin

Product NDC

0781-5177

11-digit product format

007815177

Labeler code

0781

Product ID

0781-5177_206ad017-3b96-4732-9366-1906c9dbf957

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ribavirin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA077743

Marketing category

ANDA

Marketing start

2006-10-03

Marketing end

0000-00-00

Substance

RIBAVIRIN

Active strength

200 mg/1

Pharmacologic classes

Nucleoside Analog [EXT],Nucleoside Analog Antiviral [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record