Ranitidine 150

Product NDC
49035-404
11-digit product format
490350404
Labeler code
49035
Product ID
49035-404_d109f800-f9dc-6667-fbae-7929c4d1c8d3
Type
HUMAN OTC DRUG
Nonproprietary name
Ranitidine Hydrochloride Tablets 150mg
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Walmart Stores 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#

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-404RANITIDINE 150 (RANITIDINE HYDROCHLORIDE TABLETS 150MG) TABLET, COATED [WALMART STORES INC.]4Legacy NDC20231103_83fd081b-30ae-68b4-5153-20d83caca0c1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-404-13490350404132 BOTTLE in 1 CARTON (49035-404-13) > 65 TABLET, COATED in 1 BOTTLE2 bottle2018-06-080000-00-00NoNoCurrent
49035-404-34490350404341 BOTTLE in 1 CARTON (49035-404-34) > 24 TABLET, COATED in 1 BOTTLE1 bottle2010-01-050000-00-00NoNoCurrent
49035-404-61490350404611 BOTTLE in 1 CARTON (49035-404-61) > 65 TABLET, COATED in 1 BOTTLE1 bottle2010-01-050000-00-00NoNoCurrent
49035-404-65490350404651 BOTTLE in 1 CARTON (49035-404-65) > 220 TABLET, COATED in 1 BOTTLE1 bottle2010-01-050000-00-00NoNoCurrent