basic care acid reducer

Product NDC
0113-7950
11-digit product format
001137950
Labeler code
0113
Product ID
0113-7950_99590679-57f0-46e4-a7ae-600de1b09c9e
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
2018-10-11
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
0113-7950-01001137950011 BOTTLE in 1 CARTON (0113-7950-01) > 95 TABLET, FILM COATED in 1 BOTTLE1 bottle2018-10-110000-00-00NoNoCurrent
0113-7950-09001137950091 BOTTLE in 1 CARTON (0113-7950-09) > 65 TABLET, FILM COATED in 1 BOTTLE1 bottle2018-12-300000-00-00NoNoCurrent