rabeprazole sodium

Generic: rabeprazole sodium

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rabeprazole sodium
Generic Name rabeprazole sodium
Labeler lannett company, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

rabeprazole sodium 20 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 62175-302
Product ID 62175-302_dde0e5ce-043b-4ada-aa94-eab41e41bc17
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 62175302
Hyphenated Format 62175-302

Supplemental Identifiers

RxCUI
854868
UPC
0362175302328
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 sodium (source: ndc)
Application Number ANDA090678 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-32)
  • 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-41)
  • 250 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-42)
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-43)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-46)
source: ndc

Packages (5)

62175-302-32 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-32) 62175-302-41 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-41) 62175-302-42 250 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-42) 62175-302-43 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-43) 62175-302-46 90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-46)

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": "dde0e5ce-043b-4ada-aa94-eab41e41bc17", "openfda": {"upc": ["0362175302328"], "unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["7f7d68f0-972b-4315-b712-0bb8a84c85cc"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-32)", "package_ndc": "62175-302-32", "marketing_start_date": "20131108"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-41)", "package_ndc": "62175-302-41", "marketing_start_date": "20131108"}, {"sample": false, "description": "250 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-42)", "package_ndc": "62175-302-42", "marketing_start_date": "20131108"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-43)", "package_ndc": "62175-302-43", "marketing_start_date": "20131108"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-302-46)", "package_ndc": "62175-302-46", "marketing_start_date": "20131108"}], "brand_name": "Rabeprazole Sodium", "product_id": "62175-302_dde0e5ce-043b-4ada-aa94-eab41e41bc17", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62175-302", "generic_name": "Rabeprazole Sodium", "labeler_name": "Lannett Company, 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"}