pantoprazole sodium

Generic: pantoprazole

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

Drug Facts

Product Profile

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

pantoprazole sodium 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5794
Product ID 50090-5794_2e3af5aa-2ecf-42b3-944e-ce46273f8349
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202882
Listing Expiration 2026-12-31
Marketing Start 2014-09-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905794
Hyphenated Format 50090-5794

Supplemental Identifiers

RxCUI
314200
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 (source: ndc)
Application Number ANDA202882 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-0)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-1)
source: ndc

Packages (2)

50090-5794-0 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-0) 50090-5794-1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-1)

Ingredients (1)

pantoprazole sodium (40 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": "2e3af5aa-2ecf-42b3-944e-ce46273f8349", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["3a8fa326-ad75-4b6d-8832-0a2357eeca2f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-0)", "package_ndc": "50090-5794-0", "marketing_start_date": "20211011"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-1)", "package_ndc": "50090-5794-1", "marketing_start_date": "20211011"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "50090-5794_2e3af5aa-2ecf-42b3-944e-ce46273f8349", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-5794", "generic_name": "PANTOPRAZOLE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}