Ranitidine

Product NDC

70518-0801

11-digit product format

705180801

Labeler code

70518

Product ID

70518-0801_8ecb6ac3-d947-8076-e053-2a95a90ae831

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078542

Marketing category

ANDA

Marketing start

2017-10-20

Marketing end

0000-00-00

Substance

RANITIDINE HYDROCHLORIDE

Active strength

150 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