rabeprazole sodium

Generic: rabeprazole sodium

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rabeprazole sodium
Generic Name rabeprazole sodium
Labeler direct rx
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

rabeprazole sodium 20 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-169
Product ID 72189-169_2be9206c-ed86-e301-e063-6294a90a43a8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208644
Listing Expiration 2026-12-31
Marketing Start 2021-01-14

Pharmacologic Class

Classes
proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189169
Hyphenated Format 72189-169

Supplemental Identifiers

RxCUI
854868
UNII
3L36P16U4R

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name rabeprazole sodium (source: ndc)
Generic Name rabeprazole sodium (source: ndc)
Application Number ANDA208644 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-30)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-60)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-90)
source: ndc

Packages (3)

72189-169-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-30) 72189-169-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-60) 72189-169-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-90)

Ingredients (1)

rabeprazole sodium (20 mg/1)

Linked Drug Pages (1)

RABEPRAZOLE SODIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be9206c-ed86-e301-e063-6294a90a43a8", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["b1b7def0-834f-37f5-e053-2a95a90ade1f"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-30)", "package_ndc": "72189-169-30", "marketing_start_date": "20210114"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-60)", "package_ndc": "72189-169-60", "marketing_start_date": "20210114"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-90)", "package_ndc": "72189-169-90", "marketing_start_date": "20210114"}], "brand_name": "RABEPRAZOLE SODIUM", "product_id": "72189-169_2be9206c-ed86-e301-e063-6294a90a43a8", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72189-169", "generic_name": "RABEPRAZOLE SODIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RABEPRAZOLE SODIUM", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA208644", "marketing_category": "ANDA", "marketing_start_date": "20210114", "listing_expiration_date": "20261231"}