pantoprazole sodium

Generic: pantoprazole

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

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole
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 72789-268
Product ID 72789-268_4bad4f9b-8b65-9a6d-e063-6294a90a8930
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202882
Listing Expiration 2027-12-31
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 72789268
Hyphenated Format 72789-268

Supplemental Identifiers

RxCUI
314200
UPC
0372789268309
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, PLASTIC (72789-268-30)
source: ndc

Packages (1)

72789-268-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-268-30)

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": "4bad4f9b-8b65-9a6d-e063-6294a90a8930", "openfda": {"upc": ["0372789268309"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["c1f37929-a981-4ace-95e6-ae6795a797b3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-268-30)", "package_ndc": "72789-268-30", "marketing_start_date": "20220812"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "72789-268_4bad4f9b-8b65-9a6d-e063-6294a90a8930", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72789-268", "generic_name": "PANTOPRAZOLE", "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": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20271231"}