Package 0008-0844-02

{"route": ["ORAL"], "spl_id": "c0e1404b-eca3-4219-8a1c-72a84f0f39b9", "openfda": {"upc": ["0300080843819", "0300080841815"], "unii": ["6871619Q5X"], "rxcui": ["251872", "284400", "314200", "352125", "763306", "763308"], "spl_set_id": ["08098cb2-c048-4640-f387-6beec4a38936"], "manufacturer_name": ["Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (0008-0844-02)  / 1 GRANULE, DELAYED RELEASE in 1 PACKET (0008-0844-01)", "package_ndc": "0008-0844-02", "marketing_start_date": "20080229"}], "brand_name": "Protonix Delayed-Release", "product_id": "0008-0844_c0e1404b-eca3-4219-8a1c-72a84f0f39b9", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0008-0844", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Protonix", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "NDA022020", "marketing_category": "NDA", "marketing_start_date": "20080229", "listing_expiration_date": "20261231"}