pantoprazole sodium
Generic: pantoprazole sodium
Labeler: ncs healthcare of ky, llc dba vangard labsDrug Facts
Product Profile
Brand Name
pantoprazole sodium
Generic Name
pantoprazole sodium
Labeler
ncs healthcare of ky, llc dba vangard labs
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
pantoprazole sodium 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0615-8113
Product ID
0615-8113_ee95d143-2812-493e-85ec-1dd0deb22990
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202038
Listing Expiration
2026-12-31
Marketing Start
2012-09-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06158113
Hyphenated Format
0615-8113
Supplemental Identifiers
RxCUI
UNII
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
ANDA202038 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8113-05)
- 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8113-39)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee95d143-2812-493e-85ec-1dd0deb22990", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["1680b4ed-d5b0-4fd9-b1d1-04df6a2138be"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8113-05)", "package_ndc": "0615-8113-05", "marketing_start_date": "20221215"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8113-39)", "package_ndc": "0615-8113-39", "marketing_start_date": "20181107"}], "brand_name": "Pantoprazole Sodium", "product_id": "0615-8113_ee95d143-2812-493e-85ec-1dd0deb22990", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0615-8113", "generic_name": "Pantoprazole Sodium", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20261231"}