pantoprazole sodium

Generic: pantoprazole sodium

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

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler be pharmaceuticals inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pantoprazole sodium 40 mg/10mL

Manufacturer
BE Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71839-122
Product ID 71839-122_bad4fab9-654b-423c-87dc-25ff7a9f29d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216171
Listing Expiration 2026-12-31
Marketing Start 2022-05-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71839122
Hyphenated Format 71839-122

Supplemental Identifiers

RxCUI
283669
UPC
0371839122011
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 sodium (source: ndc)
Generic Name pantoprazole sodium (source: ndc)
Application Number ANDA216171 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/10mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (71839-122-01) / 10 mL in 1 VIAL
  • 10 CARTON in 1 PACKAGE (71839-122-10) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL
  • 25 CARTON in 1 PACKAGE (71839-122-25) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL
source: ndc

Packages (3)

71839-122-01 1 VIAL in 1 CARTON (71839-122-01) / 10 mL in 1 VIAL 71839-122-10 10 CARTON in 1 PACKAGE (71839-122-10) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL 71839-122-25 25 CARTON in 1 PACKAGE (71839-122-25) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL

Ingredients (1)

pantoprazole sodium (40 mg/10mL)

Linked Drug Pages (1)

Pantoprazole sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "bad4fab9-654b-423c-87dc-25ff7a9f29d9", "openfda": {"upc": ["0371839122011"], "unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["52d5bc28-66df-43aa-bb1a-8ac4a2a7f693"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (71839-122-01)  / 10 mL in 1 VIAL", "package_ndc": "71839-122-01", "marketing_start_date": "20220525"}, {"sample": false, "description": "10 CARTON in 1 PACKAGE (71839-122-10)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL", "package_ndc": "71839-122-10", "marketing_start_date": "20220525"}, {"sample": false, "description": "25 CARTON in 1 PACKAGE (71839-122-25)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL", "package_ndc": "71839-122-25", "marketing_start_date": "20220525"}], "brand_name": "Pantoprazole sodium", "product_id": "71839-122_bad4fab9-654b-423c-87dc-25ff7a9f29d9", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "71839-122", "generic_name": "Pantoprazole sodium", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA216171", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}