Ranitidine

Product NDC

70700-155

11-digit product format

707000155

Labeler code

70700

Product ID

70700-155_97b0294d-c6a9-a9fc-28f4-41d376e85521

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Xiromed, LLC

Application

ANDA211289

Marketing category

ANDA

Marketing start

2019-02-18

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

300 mg/1

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