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 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7512
Product ID 50090-7512_a12b8b2c-799f-4090-81be-340ac97c6920
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090074
Listing Expiration 2026-12-31
Marketing Start 2011-01-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907512
Hyphenated Format 50090-7512

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 sodium (source: ndc)
Application Number ANDA090074 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7512-0)
  • 12960 TABLET, DELAYED RELEASE in 1 CASE (50090-7512-1)
source: ndc

Packages (2)

50090-7512-0 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7512-0) 50090-7512-1 12960 TABLET, DELAYED RELEASE in 1 CASE (50090-7512-1)

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": "a12b8b2c-799f-4090-81be-340ac97c6920", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["81696241-17d5-4d35-9e59-8c28469ffd2c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7512-0)", "package_ndc": "50090-7512-0", "marketing_start_date": "20250310"}, {"sample": false, "description": "12960 TABLET, DELAYED RELEASE in 1 CASE (50090-7512-1)", "package_ndc": "50090-7512-1", "marketing_start_date": "20250310"}], "brand_name": "Pantoprazole Sodium", "product_id": "50090-7512_a12b8b2c-799f-4090-81be-340ac97c6920", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50090-7512", "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": "40 mg/1"}], "application_number": "ANDA090074", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}