NIACIN

Product NDC

57297-223

11-digit product format

572970223

Labeler code

57297

Product ID

57297-223_e9acee42-88c8-44f7-b6c5-0719c9d026bc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

NIACIN

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

LUPIN LIMITED

Application

ANDA090446

Marketing category

ANDA

Marketing start

2014-03-20

Marketing end

0000-00-00

Substance

NIACIN

Active strength

1000 mg/1

Pharmacologic classes

Nicotinic Acid [EPC],Nicotinic Acids [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record