pantoprazole sodium

Generic: pantoprazole sodium

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler northstar rxllc
Dosage Form GRANULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-317
Product ID 72603-317_4494f9d0-a1c8-477f-9b4a-f65d7637d9ec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213725
Listing Expiration 2026-12-31
Marketing Start 2024-10-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603317
Hyphenated Format 72603-317

Supplemental Identifiers

RxCUI
763306
UPC
0372603317015
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 ANDA213725 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 PACKET in 1 CARTON (72603-317-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (72603-317-01)
source: ndc

Packages (1)

72603-317-30 30 PACKET in 1 CARTON (72603-317-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (72603-317-01)

Ingredients (1)

pantoprazole sodium (40 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": "4494f9d0-a1c8-477f-9b4a-f65d7637d9ec", "openfda": {"upc": ["0372603317015"], "unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["4494f9d0-a1c8-477f-9b4a-f65d7637d9ec"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (72603-317-30)  / 1 GRANULE, DELAYED RELEASE in 1 PACKET (72603-317-01)", "package_ndc": "72603-317-30", "marketing_start_date": "20241001"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "72603-317_4494f9d0-a1c8-477f-9b4a-f65d7637d9ec", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72603-317", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA213725", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}