Niacin

Product NDC

42291-584

11-digit product format

422910584

Labeler code

42291

Product ID

42291-584_63b668ba-7a0e-2a10-e053-2a91aa0ae4e1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Niacin

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA076378

Marketing category

ANDA

Marketing start

2016-08-26

Marketing end

0000-00-00

Substance

NIACIN

Active strength

500 mg/1

Pharmacologic classes

Nicotinic Acid [EPC],Nicotinic Acids [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record