pantoprazole sodium

Generic: pantoprazole sodium

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug 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
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-7629
Product ID 0615-7629_344482ad-3ddc-4be8-9fb7-a93c355a1778
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090970
Listing Expiration 2026-12-31
Marketing Start 2011-01-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06157629
Hyphenated Format 0615-7629

Supplemental Identifiers

RxCUI
314200
UNII
6871619Q5X

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 ANDA090970 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-05)
  • 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-07)
  • 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-14)
  • 28 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-28)
  • 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7629-30) / 5 TABLET, DELAYED RELEASE in 1 BLISTER PACK
  • 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-39)
source: ndc

Packages (6)

Ingredients (1)

pantoprazole sodium (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "344482ad-3ddc-4be8-9fb7-a93c355a1778", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["6faf465b-c3a3-4ae7-9e16-1ba758f6962a"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-05)", "package_ndc": "0615-7629-05", "marketing_start_date": "20220406"}, {"sample": false, "description": "7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-07)", "package_ndc": "0615-7629-07", "marketing_start_date": "20220406"}, {"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-14)", "package_ndc": "0615-7629-14", "marketing_start_date": "20220406"}, {"sample": false, "description": "28 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-28)", "package_ndc": "0615-7629-28", "marketing_start_date": "20240424"}, {"sample": false, "description": "6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7629-30)  / 5 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0615-7629-30", "marketing_start_date": "20220411"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-7629-39)", "package_ndc": "0615-7629-39", "marketing_start_date": "20220406"}], "brand_name": "Pantoprazole Sodium", "product_id": "0615-7629_344482ad-3ddc-4be8-9fb7-a93c355a1778", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0615-7629", "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": "40 mg/1"}], "application_number": "ANDA090970", "marketing_category": "ANDA", "marketing_start_date": "20110119", "listing_expiration_date": "20261231"}