Acid Reducer

Product NDC
69842-293
11-digit product format
698420293
Labeler code
69842
Product ID
69842-293_5c42e19d-3e12-4a80-8dea-0184dd03ffca
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine
Dosage form
TABLET, COATED
Route
ORAL
Labeler
CVS Pharmacy
Application
ANDA076195
Marketing category
ANDA
Marketing start
2018-05-25
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69842-293-06EA - Each69842-293b9cce503-ee94-423e-9016-dcd99b30a3fe12019-07-02
69842-293-27EA - Each69842-2934f36a61a-6f72-4cbb-b99c-d0e24d22e12c12019-07-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-293-06698420293061 BOTTLE in 1 CARTON (69842-293-06) > 160 TABLET, COATED in 1 BOTTLE1 bottle2018-05-300000-00-00NoNoCurrent
69842-293-27698420293271 BOTTLE in 1 CARTON (69842-293-27) > 80 TABLET, COATED in 1 BOTTLE1 bottle2018-05-290000-00-00NoNoCurrent
69842-293-65698420293651 BOTTLE in 1 CARTON (69842-293-65) > 30 TABLET, COATED in 1 BOTTLE1 bottle2018-05-250000-00-00NoNoCurrent