RANITIDINE

Product NDC

70408-141

11-digit product format

704080141

Labeler code

70408

Product ID

70408-141_cb826710-66c8-436e-9c7f-e47ab8e41fab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

RANITIDINE

Dosage form

SYRUP

Route

ORAL

Labeler

Nostrum Laboratories, Inc.

Application

ANDA091091

Marketing category

ANDA

Marketing start

2011-10-03

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

15 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record