pantoprazole sodium
Generic: pantoprazole sodium
Labeler: ajanta pharma usa inc.Drug Facts
Product Profile
Brand Name
pantoprazole sodium
Generic Name
pantoprazole sodium
Labeler
ajanta pharma usa inc.
Dosage Form
FOR SUSPENSION
Routes
Active Ingredients
pantoprazole sodium 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
27241-256
Product ID
27241-256_d0fe5d1b-fb0c-4c7b-af8b-cda49f2c8f7e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217416
Listing Expiration
2027-12-31
Marketing Start
2023-02-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
27241256
Hyphenated Format
27241-256
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA217416 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 1 FOR SUSPENSION in 1 PACKET (27241-256-11)
- 30 FOR SUSPENSION in 1 CARTON (27241-256-38)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d0fe5d1b-fb0c-4c7b-af8b-cda49f2c8f7e", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["90963a38-f629-45a4-bddd-9e13a55fe0f7"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 FOR SUSPENSION in 1 PACKET (27241-256-11)", "package_ndc": "27241-256-11", "marketing_start_date": "20230209"}, {"sample": false, "description": "30 FOR SUSPENSION in 1 CARTON (27241-256-38)", "package_ndc": "27241-256-38", "marketing_start_date": "20230209"}], "brand_name": "Pantoprazole sodium", "product_id": "27241-256_d0fe5d1b-fb0c-4c7b-af8b-cda49f2c8f7e", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "27241-256", "generic_name": "Pantoprazole sodium", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA217416", "marketing_category": "ANDA", "marketing_start_date": "20230209", "listing_expiration_date": "20271231"}