nizatidine

Product NDC

0185-0300

11-digit product format

001850300

Labeler code

0185

Product ID

0185-0300_b68bb8c1-f574-4c91-8b79-d1296ae7e34c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

nizatidine

Dosage form

CAPSULE

Route

ORAL

Labeler

Eon Labs, Inc.

Application

ANDA076178

Marketing category

ANDA

Marketing start

2002-07-05

Marketing end

2019-09-30

Substance

NIZATIDINE

Active strength

300 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record