Rabeprazole Sodium DR (Page 7 of 7)

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Rabeprazole #30

Rabeprazole #60Rabeprazole #30Rabeprazole #60
RABEPRAZOLE SODIUM DR rabeprazole sodium tablet, delayed release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:80425-0134(NDC:67877-443)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RABEPRAZOLE SODIUM (RABEPRAZOLE) RABEPRAZOLE SODIUM 20 mg
Product Characteristics
Color yellow Score no score
Shape ROUND Size 8mm
Flavor Imprint Code 20
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:80425-0134-2 60 TABLET, DELAYED RELEASE in 1 BOTTLE None
2 NDC:80425-0134-1 30 TABLET, DELAYED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA208644 04/27/2018
Labeler — Advanced Rx Pharmacy of Tennessee, LLC (117023142)
Establishment
Name Address ID/FEI Operations
Advanced Rx Pharmacy of Tennessee, LLC 117023142 repack (80425-0134)

Revised: 11/2021 Advanced Rx Pharmacy of Tennessee, LLC

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