rabeprazole sodium

Generic: rabeprazole sodium

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rabeprazole sodium
Generic Name rabeprazole sodium
Labeler golden state medical supply, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

rabeprazole sodium 20 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 51407-184
Product ID 51407-184_163e20cc-f058-9b74-e063-6294a90a0a3d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090678
Listing Expiration 2026-12-31
Marketing Start 2013-11-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51407184
Hyphenated Format 51407-184

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 ANDA090678 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 500 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-184-05)
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-184-30)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-184-90)
source: ndc

Packages (3)

Ingredients (1)

rabeprazole sodium (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "163e20cc-f058-9b74-e063-6294a90a0a3d", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["87231460-8b1e-b995-e053-2a91aa0a6c43"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-184-05)", "package_ndc": "51407-184-05", "marketing_start_date": "20190425"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-184-30)", "package_ndc": "51407-184-30", "marketing_start_date": "20190425"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-184-90)", "package_ndc": "51407-184-90", "marketing_start_date": "20190425"}], "brand_name": "Rabeprazole Sodium", "product_id": "51407-184_163e20cc-f058-9b74-e063-6294a90a0a3d", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "51407-184", "generic_name": "Rabeprazole Sodium", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rabeprazole Sodium", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA090678", "marketing_category": "ANDA", "marketing_start_date": "20131108", "listing_expiration_date": "20261231"}