pantoprazole sodium

Generic: pantoprazole sodium

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

Drug Facts

Product Profile

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

pantoprazole sodium 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5361
Product ID 50090-5361_7becc541-9068-4c11-9211-e000b9e57ee6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202038
Listing Expiration 2026-12-31
Marketing Start 2012-09-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905361
Hyphenated Format 50090-5361

Supplemental Identifiers

RxCUI
251872
UNII
6871619Q5X

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 pantoprazole sodium (source: ndc)
Generic Name pantoprazole sodium (source: ndc)
Application Number ANDA202038 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-0)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-1)
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-2)
source: ndc

Packages (3)

50090-5361-0 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-0) 50090-5361-1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-1) 50090-5361-2 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-2)

Ingredients (1)

pantoprazole sodium (20 mg/1)

Linked Drug Pages (1)

Pantoprazole Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7becc541-9068-4c11-9211-e000b9e57ee6", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["517d6b02-0e68-4d6b-98b3-eac0be457e6b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-0)", "package_ndc": "50090-5361-0", "marketing_start_date": "20201113"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-1)", "package_ndc": "50090-5361-1", "marketing_start_date": "20201113"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-2)", "package_ndc": "50090-5361-2", "marketing_start_date": "20201113"}], "brand_name": "Pantoprazole Sodium", "product_id": "50090-5361_7becc541-9068-4c11-9211-e000b9e57ee6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-5361", "generic_name": "Pantoprazole Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20261231"}