Acid Reducer

Product NDC
49781-027
11-digit product format
497810027
Labeler code
49781
Product ID
49781-027_5fe5c89e-ca10-4981-9899-e42e2884628c
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine
Dosage form
TABLET
Route
ORAL
Labeler
Cardinal Health
Application
ANDA200536
Marketing category
ANDA
Marketing start
2013-09-25
Marketing end
0000-00-00
Substance
RANITIDINE HYDROCHLORIDE
Active strength
150 mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49781-027-242025-05-12C16284748780-19d75b9cf-f197-f424-e053-dadaa90a57cef116b0bb-3bda-421a-ba40-827c56c1ca9c
49781-027-242020-01-31C16284748780-19d75b9cf-f197-f424-e053-dadaa90a57cef116b0bb-3bda-421a-ba40-827c56c1ca9c