Good Sense Acid Reducer

Product NDC
0113-0852
11-digit product format
001130852
Labeler code
0113
Product ID
0113-0852_8a95b38f-4958-4ab6-9c73-ba2e6bab18a0
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
L. Perrigo Company
Application
ANDA091429
Marketing category
ANDA
Marketing start
2014-02-05
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
0113-0852-02001130852021 BOTTLE in 1 CARTON (0113-0852-02) > 24 TABLET, FILM COATED in 1 BOTTLE1 bottle2015-02-050000-00-00NoNoCurrent
0113-0852-51001130852518 BLISTER PACK in 1 CARTON (0113-0852-51) > 1 TABLET, FILM COATED in 1 BLISTER PACK8 blister pack2016-08-100000-00-00NoNoCurrent
0113-0852-620011308526224 BLISTER PACK in 1 CARTON (0113-0852-62) > 1 TABLET, FILM COATED in 1 BLISTER PACK24 blister pack2015-02-050000-00-00NoNoCurrent
0113-0852-71001130852711 BOTTLE in 1 CARTON (0113-0852-71) > 50 TABLET, FILM COATED in 1 BOTTLE1 bottle2015-02-050000-00-00NoNoCurrent