rabeprazole sodium

Generic: rabeprazole sodium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

rabeprazole sodium 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-555
Product ID 63187-555_45879472-a15c-4577-8df5-a2fbd9c5173d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202376
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 63187555
Hyphenated Format 63187-555

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 ANDA202376 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-30)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-60)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-90)
source: ndc

Packages (3)

63187-555-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-30) 63187-555-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-60) 63187-555-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-90)

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": "45879472-a15c-4577-8df5-a2fbd9c5173d", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["d1444508-fe40-4f68-8350-52f13399e38a"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-30)", "package_ndc": "63187-555-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-60)", "package_ndc": "63187-555-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-555-90)", "package_ndc": "63187-555-90", "marketing_start_date": "20181201"}], "brand_name": "Rabeprazole sodium", "product_id": "63187-555_45879472-a15c-4577-8df5-a2fbd9c5173d", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "63187-555", "generic_name": "Rabeprazole sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rabeprazole sodium", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202376", "marketing_category": "ANDA", "marketing_start_date": "20131108", "listing_expiration_date": "20261231"}