rabeprazole sodium

Generic: rabeprazole sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rabeprazole sodium
Generic Name rabeprazole sodium
Labeler a-s medication solutions
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

rabeprazole sodium 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4751
Product ID 50090-4751_e50376c6-3db4-429f-bf11-982f49d5e4df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208644
Listing Expiration 2026-12-31
Marketing Start 2018-04-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904751
Hyphenated Format 50090-4751

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 (50090-4751-0)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-1)
source: ndc

Packages (2)

50090-4751-0 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-0) 50090-4751-1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-1)

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": "e50376c6-3db4-429f-bf11-982f49d5e4df", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["4ded337a-31b8-47c3-b5ab-33a785afb7d8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-0)", "package_ndc": "50090-4751-0", "marketing_start_date": "20191125"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-1)", "package_ndc": "50090-4751-1", "marketing_start_date": "20191125"}], "brand_name": "Rabeprazole Sodium", "product_id": "50090-4751_e50376c6-3db4-429f-bf11-982f49d5e4df", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-4751", "generic_name": "Rabeprazole Sodium", "labeler_name": "A-S Medication Solutions", "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": "20180427", "listing_expiration_date": "20261231"}