pantoprazole sodium

Generic: pantoprazole sodium

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler american health packaging
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 20 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-725
Product ID 60687-725_228dc54a-3313-71e5-e063-6394a90a5bb0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202038
Listing Expiration 2026-12-31
Marketing Start 2023-07-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687725
Hyphenated Format 60687-725

Supplemental Identifiers

RxCUI
251872 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 ANDA202038 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-725-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-725-11)
source: ndc

Packages (1)

60687-725-01 100 BLISTER PACK in 1 CARTON (60687-725-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-725-11)

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": "228dc54a-3313-71e5-e063-6394a90a5bb0", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["5ff3cf6c-6f0a-4374-8b80-4e1eb1df6245"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-725-01)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-725-11)", "package_ndc": "60687-725-01", "marketing_start_date": "20230705"}], "brand_name": "Pantoprazole Sodium", "product_id": "60687-725_228dc54a-3313-71e5-e063-6394a90a5bb0", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "60687-725", "generic_name": "Pantoprazole Sodium", "labeler_name": "American Health Packaging", "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": "20230705", "listing_expiration_date": "20261231"}