rabeprazole sodium

Generic: rabeprazole

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rabeprazole sodium
Generic Name rabeprazole
Labeler amneal pharmaceuticals llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

rabeprazole sodium 20 mg/1

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 65162-724
Product ID 65162-724_f02b0373-dbac-4842-bf97-3352b8c74089
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204179
Listing Expiration 2026-12-31
Marketing Start 2015-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65162724
Hyphenated Format 65162-724

Supplemental Identifiers

RxCUI
854868
UPC
0365162724035
UNII
3L36P16U4R

Packaging Origin

Original Packager
true

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 (source: ndc)
Application Number ANDA204179 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-03)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-09)
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-11)
  • 500 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-50)
source: ndc

Packages (4)

65162-724-03 30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-03) 65162-724-09 90 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-09) 65162-724-11 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-11) 65162-724-50 500 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-50)

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": "f02b0373-dbac-4842-bf97-3352b8c74089", "openfda": {"upc": ["0365162724035"], "unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["951caefe-6e18-48ff-9567-beb545b09c25"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-03)", "package_ndc": "65162-724-03", "marketing_start_date": "20151001"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-09)", "package_ndc": "65162-724-09", "marketing_start_date": "20151001"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-11)", "package_ndc": "65162-724-11", "marketing_start_date": "20151001"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-724-50)", "package_ndc": "65162-724-50", "marketing_start_date": "20151001"}], "brand_name": "Rabeprazole Sodium", "product_id": "65162-724_f02b0373-dbac-4842-bf97-3352b8c74089", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "65162-724", "generic_name": "Rabeprazole", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rabeprazole Sodium", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA204179", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}