Package 16571-856-01

{"route": ["ORAL"], "spl_id": "06c53ec5-f3d9-47e2-943e-631ed695adcc", "openfda": {"nui": ["N0000175895", "N0000009065"], "upc": ["0316571856503"], "unii": ["SD6QCT3TSU"], "rxcui": ["312301"], "spl_set_id": ["cd840a2c-2a0e-4b2b-84ff-a0406bb6fa37"], "pharm_class_pe": ["Hematologic Activity Alteration [PE]"], "pharm_class_epc": ["Blood Viscosity Reducer [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-856-01)", "package_ndc": "16571-856-01", "marketing_start_date": "20240611"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-856-50)", "package_ndc": "16571-856-50", "marketing_start_date": "20240611"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (16571-856-90)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "16571-856-90", "marketing_start_date": "20240611"}], "brand_name": "Pentoxifylline", "product_id": "16571-856_06c53ec5-f3d9-47e2-943e-631ed695adcc", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Blood Viscosity Reducer [EPC]", "Hematologic Activity Alteration [PE]"], "product_ndc": "16571-856", "generic_name": "Pentoxifylline", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pentoxifylline", "active_ingredients": [{"name": "PENTOXIFYLLINE", "strength": "400 mg/1"}], "application_number": "ANDA074425", "marketing_category": "ANDA", "marketing_start_date": "20240611", "listing_expiration_date": "20261231"}