pantoprazole sodium

Generic: pantoprazole sodium

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-086
Product ID 72789-086_4031c357-7001-521b-e063-6294a90a232c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078281
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 72789086
Hyphenated Format 72789-086

Supplemental Identifiers

RxCUI
314200
UPC
0372789086309
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 ANDA078281 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-086-30)
source: ndc

Packages (1)

72789-086-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-086-30)

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": "4031c357-7001-521b-e063-6294a90a232c", "openfda": {"upc": ["0372789086309"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["b422c5eb-9a6d-4f8c-863d-ca515ec780c2"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-086-30)", "package_ndc": "72789-086-30", "marketing_start_date": "20200604"}], "brand_name": "Pantoprazole Sodium", "product_id": "72789-086_4031c357-7001-521b-e063-6294a90a232c", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72789-086", "generic_name": "Pantoprazole Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA078281", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}