Package 62756-071-64

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 62756-071-64
Digits Only 6275607164
Product NDC 62756-071
Description

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

Marketing

Marketing Status
Marketed Since 2020-07-01
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

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"}