Ranitidine

Product NDC

60505-4623

11-digit product format

605054623

Labeler code

60505

Product ID

60505-4623_79026753-b4f6-b094-f0f3-156492d41412

Type

HUMAN OTC DRUG

Nonproprietary name

Ranitidine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Apotex Corp.

Application

ANDA200172

Marketing category

ANDA

Marketing start

2017-07-27

Marketing end

2020-10-31

Substance

RANITIDINE HYDROCHLORIDE

Active strength

150 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record