Package 42708-104-30

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package Sample

Package Facts

Identity

Package NDC 42708-104-30
Digits Only 4270810430
Product NDC 42708-104
Product ID 42708-104_459c8b98-1e98-7bad-e063-6394a90aaf17
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (42708-104-30)

Marketing

Marketing Status
Marketed Since 2019-11-18
Brand pantoprazole sodium
Generic pantoprazole
Sample Package Yes

Linked Drug Pages (1)

PANTOPRAZOLE SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459c8b98-1e98-7bad-e063-6394a90aaf17", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["b4a94a37-47c1-4dd9-9e4d-5b4a03480aa6"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (42708-104-30)", "package_ndc": "42708-104-30", "marketing_start_date": "20191118"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "42708-104_459c8b98-1e98-7bad-e063-6394a90aaf17", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "42708-104", "generic_name": "PANTOPRAZOLE", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}