pantoprazole sodium

Generic: pantoprazole

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 20 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2285
Product ID 68071-2285_1d783072-b076-e384-e063-6394a90a7460
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202882
Listing Expiration 2026-12-31
Marketing Start 2014-09-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712285
Hyphenated Format 68071-2285

Supplemental Identifiers

RxCUI
251872
UPC
0368071228564
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 (source: ndc)
Application Number ANDA202882 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2285-6)
source: ndc

Packages (1)

68071-2285-6 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2285-6)

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": "1d783072-b076-e384-e063-6394a90a7460", "openfda": {"upc": ["0368071228564"], "unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["b2abc159-e450-99dc-e053-2a95a90abe6a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2285-6)", "package_ndc": "68071-2285-6", "marketing_start_date": "20201027"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "68071-2285_1d783072-b076-e384-e063-6394a90a7460", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-2285", "generic_name": "PANTOPRAZOLE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}