pantoprazole sodium
Generic: pantoprazole sodium
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
pantoprazole sodium
Generic Name
pantoprazole sodium
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
pantoprazole sodium 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9284
Product ID
0143-9284_284915b9-082e-4c76-8998-13aff7221045
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA209463
Listing Expiration
2026-12-31
Marketing Start
2017-09-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439284
Hyphenated Format
0143-9284
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
NDA209463 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 10 VIAL in 1 CARTON (0143-9284-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9284-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "284915b9-082e-4c76-8998-13aff7221045", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["b02f3f85-8f9b-4d06-8eae-73e592626f3e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9284-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9284-01)", "package_ndc": "0143-9284-10", "marketing_start_date": "20170922"}], "brand_name": "Pantoprazole Sodium", "product_id": "0143-9284_284915b9-082e-4c76-8998-13aff7221045", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0143-9284", "generic_name": "Pantoprazole Sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "NDA209463", "marketing_category": "NDA", "marketing_start_date": "20170922", "listing_expiration_date": "20261231"}