pantoprazole sodium delayed-release

Generic: pantoprazole sodium delayed-release

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium delayed-release
Generic Name pantoprazole sodium delayed-release
Labeler lifestar pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pantoprazole sodium 20 mg/1

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-018
Product ID 70756-018_2c507c43-c033-4b6e-b954-f0f2fb617289
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215880
Listing Expiration 2026-12-31
Marketing Start 2024-04-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70756018
Hyphenated Format 70756-018

Supplemental Identifiers

RxCUI
251872 314200
UPC
0370756019121 0370756019909
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 delayed-release (source: ndc)
Generic Name pantoprazole sodium delayed-release (source: ndc)
Application Number ANDA215880 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (70756-018-51)
  • 90 TABLET in 1 BOTTLE (70756-018-90)
source: ndc

Packages (2)

70756-018-51 500 TABLET in 1 BOTTLE (70756-018-51) 70756-018-90 90 TABLET in 1 BOTTLE (70756-018-90)

Ingredients (1)

pantoprazole sodium (20 mg/1)

Linked Drug Pages (1)

Pantoprazole sodium delayed-release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c507c43-c033-4b6e-b954-f0f2fb617289", "openfda": {"upc": ["0370756019121", "0370756019909"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["0502f935-af7a-4f1e-8c3e-29e20647c885"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (70756-018-51)", "package_ndc": "70756-018-51", "marketing_start_date": "20240425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70756-018-90)", "package_ndc": "70756-018-90", "marketing_start_date": "20240425"}], "brand_name": "Pantoprazole sodium delayed-release", "product_id": "70756-018_2c507c43-c033-4b6e-b954-f0f2fb617289", "dosage_form": "TABLET", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70756-018", "generic_name": "Pantoprazole sodium delayed-release", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole sodium delayed-release", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA215880", "marketing_category": "ANDA", "marketing_start_date": "20240425", "listing_expiration_date": "20261231"}