Ranitidine

Product NDC

60760-249

11-digit product format

607600249

Labeler code

60760

Product ID

60760-249_a2f6a5cf-8876-8bc4-e053-2995a90acfad

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ranitidine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

St. Mary's Medical Park Pharmacy

Application

ANDA078542

Marketing category

ANDA

Marketing start

2008-11-19

Marketing end

2021-01-31

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