pantoprazole sodium

Generic: pantoprazole sodium

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

Drug Facts

Product Profile

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

pantoprazole sodium 20 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-190
Product ID 70010-190_451bb2fa-e53b-6104-e063-6294a90afd37
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217282
Listing Expiration 2026-12-31
Marketing Start 2024-04-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70010190
Hyphenated Format 70010-190

Supplemental Identifiers

RxCUI
251872 314200
UPC
0370010191099
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 ANDA217282 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-09)
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-10)
source: ndc

Packages (2)

70010-190-09 90 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-09) 70010-190-10 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-10)

Ingredients (1)

pantoprazole sodium (20 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": "451bb2fa-e53b-6104-e063-6294a90afd37", "openfda": {"upc": ["0370010191099"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["8f2fb647-15bc-41cb-84a4-02e956e614fc"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-09)", "package_ndc": "70010-190-09", "marketing_start_date": "20240412"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-10)", "package_ndc": "70010-190-10", "marketing_start_date": "20240412"}], "brand_name": "pantoprazole sodium", "product_id": "70010-190_451bb2fa-e53b-6104-e063-6294a90afd37", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70010-190", "generic_name": "pantoprazole sodium", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "pantoprazole sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA217282", "marketing_category": "ANDA", "marketing_start_date": "20240412", "listing_expiration_date": "20261231"}