pantoprazole sodium

Generic: pantoprazole sodium

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

Drug Facts

Product Profile

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

pantoprazole sodium 40 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-1963
Product ID 68071-1963_1d4be162-1637-896d-e063-6394a90a39f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090074
Listing Expiration 2026-12-31
Marketing Start 2011-01-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680711963
Hyphenated Format 68071-1963

Supplemental Identifiers

RxCUI
314200
UPC
0368071196344
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 ANDA090074 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-3)
  • 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-4)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-6)
source: ndc

Packages (3)

68071-1963-3 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-3) 68071-1963-4 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-4) 68071-1963-6 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-6)

Ingredients (1)

pantoprazole sodium (40 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": "1d4be162-1637-896d-e063-6394a90a39f0", "openfda": {"upc": ["0368071196344"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["4fbec80c-b38d-122c-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-3)", "package_ndc": "68071-1963-3", "marketing_start_date": "20110120"}, {"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-4)", "package_ndc": "68071-1963-4", "marketing_start_date": "20110120"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-1963-6)", "package_ndc": "68071-1963-6", "marketing_start_date": "20110120"}], "brand_name": "Pantoprazole Sodium", "product_id": "68071-1963_1d4be162-1637-896d-e063-6394a90a39f0", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-1963", "generic_name": "Pantoprazole Sodium", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA090074", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}