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 FOR SUSPENSION
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-767
Product ID 60687-767_236c62bf-3ddb-0b3e-e063-6394a90ad6c6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217416
Listing Expiration 2026-12-31
Marketing Start 2023-08-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687767
Hyphenated Format 60687-767

Supplemental Identifiers

RxCUI
763306
UNII
6871619Q5X

Packaging Origin

Original Packager
true

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 ANDA217416 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 PACKET in 1 CARTON (60687-767-27) / 1 FOR SUSPENSION in 1 PACKET (60687-767-99)
source: ndc

Packages (1)

Ingredients (1)

pantoprazole sodium (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "236c62bf-3ddb-0b3e-e063-6394a90ad6c6", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["423dac8b-bb1e-4456-9b6e-913c028b11bc"], "manufacturer_name": ["American Health Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (60687-767-27)  / 1 FOR SUSPENSION in 1 PACKET (60687-767-99)", "package_ndc": "60687-767-27", "marketing_start_date": "20230801"}], "brand_name": "Pantoprazole sodium", "product_id": "60687-767_236c62bf-3ddb-0b3e-e063-6394a90ad6c6", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "60687-767", "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": "40 mg/1"}], "application_number": "ANDA217416", "marketing_category": "ANDA", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}