protonix delayed-release

Generic: pantoprazole sodium

Labeler: wyeth pharmaceuticals llc, a subsidiary of pfizer inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name protonix delayed-release
Generic Name pantoprazole sodium
Labeler wyeth pharmaceuticals llc, a subsidiary of pfizer inc.
Dosage Form GRANULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

Identifiers & Regulatory

Product NDC 0008-0844
Product ID 0008-0844_c0e1404b-eca3-4219-8a1c-72a84f0f39b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022020
Listing Expiration 2026-12-31
Marketing Start 2008-02-29

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00080844
Hyphenated Format 0008-0844

Supplemental Identifiers

RxCUI
251872 284400 314200 352125 763306 763308
UPC
0300080843819 0300080841815
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 protonix delayed-release (source: ndc)
Generic Name pantoprazole sodium (source: ndc)
Application Number NDA022020 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 PACKET in 1 CARTON (0008-0844-02) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (0008-0844-01)
source: ndc

Packages (1)

0008-0844-02 30 PACKET in 1 CARTON (0008-0844-02) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (0008-0844-01)

Ingredients (1)

pantoprazole sodium (40 mg/1)

Linked Drug Pages (1)

Protonix Delayed-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c0e1404b-eca3-4219-8a1c-72a84f0f39b9", "openfda": {"upc": ["0300080843819", "0300080841815"], "unii": ["6871619Q5X"], "rxcui": ["251872", "284400", "314200", "352125", "763306", "763308"], "spl_set_id": ["08098cb2-c048-4640-f387-6beec4a38936"], "manufacturer_name": ["Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (0008-0844-02)  / 1 GRANULE, DELAYED RELEASE in 1 PACKET (0008-0844-01)", "package_ndc": "0008-0844-02", "marketing_start_date": "20080229"}], "brand_name": "Protonix Delayed-Release", "product_id": "0008-0844_c0e1404b-eca3-4219-8a1c-72a84f0f39b9", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0008-0844", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Protonix", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "NDA022020", "marketing_category": "NDA", "marketing_start_date": "20080229", "listing_expiration_date": "20261231"}