Package 42708-185-30

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package Sample

Package Facts

Identity

Package NDC 42708-185-30
Digits Only 4270818530
Product NDC 42708-185
Product ID 42708-185_45871cff-d99a-9f24-e063-6294a90a821f
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-185-30)

Marketing

Marketing Status
Marketed Since 2024-01-12
Brand pantoprazole sodium
Generic pantoprazole sodium
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": "45871cff-d99a-9f24-e063-6294a90a821f", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["0e200326-8885-18d0-e063-6294a90aad2f"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-185-30)", "package_ndc": "42708-185-30", "marketing_start_date": "20240112"}], "brand_name": "Pantoprazole Sodium", "product_id": "42708-185_45871cff-d99a-9f24-e063-6294a90a821f", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "42708-185", "generic_name": "Pantoprazole Sodium", "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": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20261231"}