Ranitidine 150

Product NDC
68998-375
11-digit product format
689980375
Labeler code
68998
Product ID
68998-375_81b9cd7a-0f56-454f-b843-2d3e0daa2470
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine HCl Tablets 150mg
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Marc Glassman, Inc.
Application
ANDA078192
Marketing category
ANDA
Marketing start
2010-01-05
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68998-375-932021-03-30C16284748780-1ba0f9c33-422d-a910-e053-dadaa90a0b8575970c03-1537-441d-a626-ceb2e1fe2abc
68998-375-932021-01-29C16284748780-1ba0f9c33-422d-a910-e053-dadaa90a0b8575970c03-1537-441d-a626-ceb2e1fe2abc