pantoprazole sodium
Generic: pantoprazole sodium
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
pantoprazole sodium
Generic Name
pantoprazole sodium
Labeler
american health packaging
Dosage Form
FOR SUSPENSION
Routes
Active Ingredients
pantoprazole sodium 40 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687767
Hyphenated Format
60687-767
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 PACKET in 1 CARTON (60687-767-27) / 1 FOR SUSPENSION in 1 PACKET (60687-767-99)
Packages (1)
Ingredients (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"}