pantoprazole sodium

Generic: pantoprazole sodium

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

Drug Facts

Product Profile

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

pantoprazole sodium 40 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-032
Product ID 31722-032_092a2d03-1a01-a7ac-e063-6394a90a01b4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216139
Listing Expiration 2026-12-31
Marketing Start 2023-10-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722032
Hyphenated Format 31722-032

Supplemental Identifiers

RxCUI
763306
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 ANDA216139 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 PACKET in 1 CARTON (31722-032-32) / 1 GRANULE, DELAYED RELEASE in 1 PACKET
source: ndc

Packages (1)

31722-032-32 30 PACKET in 1 CARTON (31722-032-32) / 1 GRANULE, DELAYED RELEASE in 1 PACKET

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": "092a2d03-1a01-a7ac-e063-6394a90a01b4", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["ee6278c0-d8c0-417c-a65c-b522ff76fe44"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (31722-032-32)  / 1 GRANULE, DELAYED RELEASE in 1 PACKET", "package_ndc": "31722-032-32", "marketing_start_date": "20231027"}], "brand_name": "Pantoprazole Sodium", "product_id": "31722-032_092a2d03-1a01-a7ac-e063-6394a90a01b4", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "31722-032", "generic_name": "Pantoprazole Sodium", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA216139", "marketing_category": "ANDA", "marketing_start_date": "20231027", "listing_expiration_date": "20261231"}