pantoprazole sodium

Generic: pantoprazole sodium

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler cardinal health 107, llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 20 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-2645
Product ID 55154-2645_cb2133e3-b30c-4492-b438-efc08caf3fd6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202038
Listing Expiration 2027-12-31
Marketing Start 2025-02-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551542645
Hyphenated Format 55154-2645

Supplemental Identifiers

RxCUI
251872 314200
UPC
0055154264501
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
  • 10 BLISTER PACK in 1 BAG (55154-2645-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

55154-2645-0 10 BLISTER PACK in 1 BAG (55154-2645-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

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": "cb2133e3-b30c-4492-b438-efc08caf3fd6", "openfda": {"upc": ["0055154264501"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["6229247e-ee15-466e-a8ac-adcd646b738d"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2645-0)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "55154-2645-0", "marketing_start_date": "20250225"}], "brand_name": "Pantoprazole Sodium", "product_id": "55154-2645_cb2133e3-b30c-4492-b438-efc08caf3fd6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "55154-2645", "generic_name": "Pantoprazole Sodium", "labeler_name": "Cardinal Health 107, LLC", "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": "20250225", "listing_expiration_date": "20271231"}