Ranitidine Hydrochloride

Product NDC

62559-691

11-digit product format

625590691

Labeler code

62559

Product ID

62559-691_c51f0dee-92a4-41cb-825d-20baaace7355

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

ANI Pharmaceuticals, Inc.

Application

ANDA211893

Marketing category

ANDA

Marketing start

2019-06-24

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