Ranitidine

Product NDC

50436-0291

11-digit product format

504360291

Labeler code

50436

Product ID

50436-0291_5456e371-00d0-4689-bd69-be0942714410

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

SYRUP

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA090102

Marketing category

ANDA

Marketing start

2013-07-15

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

2019-12-31

Current FDA listing

Historical FDA.report record