MAXIMUM STRENGTH RANITIDINE

Product NDC
58602-734
11-digit product format
586020734
Labeler code
58602
Product ID
58602-734_71b6ee04-198f-4a3c-823f-a93400ea6965
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine
Dosage form
TABLET
Route
ORAL
Labeler
Aurohealth LLC
Application
ANDA207578
Marketing category
ANDA
Marketing start
2017-11-13
Marketing end
0000-00-00
Substance
RANITIDINE HYDROCHLORIDE
Active strength
150 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58602-734-02586020734021 BOTTLE in 1 CARTON (58602-734-02) > 8 TABLET in 1 BOTTLE1 bottle2019-04-240000-00-00NoNoCurrent
58602-734-07586020734071 BOTTLE in 1 CARTON (58602-734-07) > 24 TABLET in 1 BOTTLE1 bottle2017-11-130000-00-00NoNoCurrent
58602-734-14586020734141 BOTTLE in 1 CARTON (58602-734-14) > 50 TABLET in 1 BOTTLE1 bottle2017-11-130000-00-00NoNoCurrent
58602-734-16586020734161 BOTTLE in 1 CARTON (58602-734-16) > 65 TABLET in 1 BOTTLE1 bottle2017-11-130000-00-00NoNoCurrent
58602-734-17586020734171 BOTTLE in 1 CARTON (58602-734-17) > 45 TABLET in 1 BOTTLE1 bottle2017-11-130000-00-00NoNoCurrent
58602-734-20586020734201 BOTTLE in 1 CARTON (58602-734-20) > 95 TABLET in 1 BOTTLE1 bottle2017-11-130000-00-00NoNoCurrent
58602-734-40586020734401 BOTTLE in 1 CARTON (58602-734-40) > 500 TABLET in 1 BOTTLE1 bottle2017-11-130000-00-00NoNoCurrent
58602-734-50586020734501 BOTTLE in 1 CARTON (58602-734-50) > 85 TABLET in 1 BOTTLE1 bottle2017-11-130000-00-00NoNoCurrent
58602-734-79586020734791 BLISTER PACK in 1 CARTON (58602-734-79) > 8 TABLET in 1 BLISTER PACK1 blister pack2019-11-120000-00-00NoNoCurrent