pantoprazole sodium

Generic: pantoprazole sodium

Labeler: edenbridge pharmaceuticals llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler edenbridge pharmaceuticals llc.
Dosage Form GRANULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Edenbridge Pharmaceuticals LLC.

Identifiers & Regulatory

Product NDC 42799-952
Product ID 42799-952_27c1732b-93f7-4c6c-941b-57223d7238ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216247
Listing Expiration 2027-12-31
Marketing Start 2023-06-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42799952
Hyphenated Format 42799-952

Supplemental Identifiers

RxCUI
763306
UPC
0342799952017
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 ANDA216247 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 PACKET in 1 CARTON (42799-952-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (42799-952-01)
source: ndc

Packages (1)

42799-952-30 30 PACKET in 1 CARTON (42799-952-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (42799-952-01)

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": "27c1732b-93f7-4c6c-941b-57223d7238ac", "openfda": {"upc": ["0342799952017"], "unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["a0bb76bc-094a-4d61-9bb2-2226c9da4ae9"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (42799-952-30)  / 1 GRANULE, DELAYED RELEASE in 1 PACKET (42799-952-01)", "package_ndc": "42799-952-30", "marketing_start_date": "20230815"}], "brand_name": "Pantoprazole Sodium", "product_id": "42799-952_27c1732b-93f7-4c6c-941b-57223d7238ac", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "42799-952", "generic_name": "Pantoprazole Sodium", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA216247", "marketing_category": "ANDA", "marketing_start_date": "20230616", "listing_expiration_date": "20271231"}