Ranitidine

Product NDC

60687-322

11-digit product format

606870322

Labeler code

60687

Product ID

60687-322_a40923c3-7358-29f3-e053-2995a90ad18f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA077824

Marketing category

ANDA

Marketing start

2017-08-18

Marketing end

2020-12-31

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

0000-00-00

Current FDA listing

Historical FDA.report record