pantoprazole

Generic: pantoprazole

Labeler: dr.reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole
Generic Name pantoprazole
Labeler dr.reddy's laboratories limited
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Dr.Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-333
Product ID 55111-333_5c22ca2e-52db-fb09-be54-ddf8c4e428c8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077619
Listing Expiration 2026-12-31
Marketing Start 2011-01-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55111333
Hyphenated Format 55111-333

Supplemental Identifiers

RxCUI
251872 314200
UNII
6871619Q5X

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name pantoprazole (source: ndc)
Application Number ANDA077619 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-01)
  • 500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-05)
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-10)
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-30)
  • 10 BLISTER PACK in 1 CARTON (55111-333-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)
  • 3 BLISTER PACK in 1 CARTON (55111-333-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-90)
source: ndc

Packages (7)

55111-333-01 100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-01) 55111-333-05 500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-05) 55111-333-10 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-10) 55111-333-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-30) 55111-333-78 10 BLISTER PACK in 1 CARTON (55111-333-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79) 55111-333-81 3 BLISTER PACK in 1 CARTON (55111-333-81) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79) 55111-333-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-90)

Ingredients (1)

pantoprazole sodium (40 mg/1)

Linked Drug Pages (1)

Pantoprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5c22ca2e-52db-fb09-be54-ddf8c4e428c8", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["564709e8-358f-c185-4ecb-b3849c3fe59c"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-01)", "package_ndc": "55111-333-01", "marketing_start_date": "20110119"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-05)", "package_ndc": "55111-333-05", "marketing_start_date": "20110119"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-10)", "package_ndc": "55111-333-10", "marketing_start_date": "20110119"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-30)", "package_ndc": "55111-333-30", "marketing_start_date": "20110119"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-333-78)  / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)", "package_ndc": "55111-333-78", "marketing_start_date": "20110119"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (55111-333-81)  / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-333-79)", "package_ndc": "55111-333-81", "marketing_start_date": "20110119"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-333-90)", "package_ndc": "55111-333-90", "marketing_start_date": "20110119"}], "brand_name": "Pantoprazole", "product_id": "55111-333_5c22ca2e-52db-fb09-be54-ddf8c4e428c8", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "55111-333", "generic_name": "Pantoprazole", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA077619", "marketing_category": "ANDA", "marketing_start_date": "20110119", "listing_expiration_date": "20261231"}