FDA NDC

NIACIN

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
47335-613
Proprietary name
NIACIN
Nonproprietary name
NIACIN
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Strength
1000 mg/1

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