pantoprazole sodium

Generic: pantoprazole sodium

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler sun pharmaceutical industries, inc.
Dosage Form GRANULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-071
Product ID 62756-071_d19d65d9-7bab-4a6f-9a79-ed3d32bd83d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213725
Listing Expiration 2026-12-31
Marketing Start 2020-07-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756071
Hyphenated Format 62756-071

Supplemental Identifiers

RxCUI
763306
UPC
0362756071643
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 (62756-071-64) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (62756-071-60)
source: ndc

Packages (1)

62756-071-64 30 PACKET in 1 CARTON (62756-071-64) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (62756-071-60)

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": "d19d65d9-7bab-4a6f-9a79-ed3d32bd83d9", "openfda": {"upc": ["0362756071643"], "unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["38353b9e-63bd-47e8-b7cb-b198d1e901f9"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (62756-071-64)  / 1 GRANULE, DELAYED RELEASE in 1 PACKET (62756-071-60)", "package_ndc": "62756-071-64", "marketing_start_date": "20200701"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "62756-071_d19d65d9-7bab-4a6f-9a79-ed3d32bd83d9", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62756-071", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "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": "20200701", "listing_expiration_date": "20261231"}