Ranitidine 75

Product NDC
30142-131
11-digit product format
301420131
Labeler code
30142
Product ID
30142-131_bc6da364-ddaa-3f79-04c8-6e39277b94da
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine Tablets USP, 75mg
Dosage form
TABLET
Route
ORAL
Labeler
The Kroger Co.
Application
ANDA075294
Marketing category
ANDA
Marketing start
2011-03-31
Marketing end
0000-00-00
Substance
RANITIDINE HYDROCHLORIDE
Active strength
75 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-131RANITIDINE 75 (RANITIDINE TABLETS USP, 75MG) TABLET [THE KROGER CO.]5Legacy NDC20231103_9589228d-1c1e-7a81-b64d-e9ca6a141a8b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-131-30301420131301 BOTTLE in 1 CARTON (30142-131-30) > 30 TABLET in 1 BOTTLE1 bottle2011-03-310000-00-00NoNoCurrent
30142-131-60301420131601 BOTTLE in 1 CARTON (30142-131-60) > 60 TABLET in 1 BOTTLE1 bottle2011-03-310000-00-00NoNoCurrent