RANITIDINE

Product NDC

60760-026

11-digit product format

607600026

Labeler code

60760

Product ID

60760-026_77e674b1-29b4-32db-e053-2991aa0a8a13

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

RANITIDINE

Dosage form

TABLET

Route

ORAL

Labeler

St Marys Medical Park Pharmacy

Application

ANDA077824

Marketing category

ANDA

Marketing start

2014-01-30

Marketing end

2019-04-30

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

0000-00-00

Current FDA listing

Historical FDA.report record