pantoprazole sodium

Generic: pantoprazole

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole
Labeler bryant ranch prepack
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0291
Product ID 71335-0291_74c908a1-9dbb-430f-adab-49d147c49e19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205119
Listing Expiration 2026-12-31
Marketing Start 2016-06-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350291
Hyphenated Format 71335-0291

Supplemental Identifiers

RxCUI
251872
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 ANDA205119 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-1)
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-2)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-3)
  • 56 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-4)
  • 28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-5)
  • 10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-6)
  • 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-7)
  • 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-8)
  • 3 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-9)
source: ndc

Packages (9)

Ingredients (1)

pantoprazole sodium (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "74c908a1-9dbb-430f-adab-49d147c49e19", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["d212e8ec-f7ff-4727-a83e-0edc4ca7e6d1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-1)", "package_ndc": "71335-0291-1", "marketing_start_date": "20220429"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-2)", "package_ndc": "71335-0291-2", "marketing_start_date": "20220524"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-3)", "package_ndc": "71335-0291-3", "marketing_start_date": "20220628"}, {"sample": false, "description": "56 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-4)", "package_ndc": "71335-0291-4", "marketing_start_date": "20220628"}, {"sample": false, "description": "28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-5)", "package_ndc": "71335-0291-5", "marketing_start_date": "20220628"}, {"sample": false, "description": "10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-6)", "package_ndc": "71335-0291-6", "marketing_start_date": "20220628"}, {"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-7)", "package_ndc": "71335-0291-7", "marketing_start_date": "20220628"}, {"sample": false, "description": "180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-8)", "package_ndc": "71335-0291-8", "marketing_start_date": "20220628"}, {"sample": false, "description": "3 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0291-9)", "package_ndc": "71335-0291-9", "marketing_start_date": "20220628"}], "brand_name": "Pantoprazole Sodium", "product_id": "71335-0291_74c908a1-9dbb-430f-adab-49d147c49e19", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "71335-0291", "generic_name": "Pantoprazole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA205119", "marketing_category": "ANDA", "marketing_start_date": "20160620", "listing_expiration_date": "20261231"}