Package 70954-668-10

Brand: pentoxifylline

Generic: pentoxifylline
NDC Package

Package Facts

Identity

Package NDC 70954-668-10
Digits Only 7095466810
Product NDC 70954-668
Product ID 70954-668_9732cf08-dad4-42a4-a10e-0284848724d7
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-10)

Marketing

Marketing Status
Marketed Since 2024-01-15
Brand pentoxifylline
Generic pentoxifylline
Sample Package No

Linked Drug Pages (1)

Pentoxifylline ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9732cf08-dad4-42a4-a10e-0284848724d7", "openfda": {"nui": ["N0000175895", "N0000009065"], "upc": ["0370954668107"], "unii": ["SD6QCT3TSU"], "rxcui": ["312301"], "spl_set_id": ["9ca79c97-e4e5-4297-85eb-7a9b3d8083b5"], "pharm_class_pe": ["Hematologic Activity Alteration [PE]"], "pharm_class_epc": ["Blood Viscosity Reducer [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-10)", "package_ndc": "70954-668-10", "marketing_start_date": "20240115"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-20)", "package_ndc": "70954-668-20", "marketing_start_date": "20240115"}], "brand_name": "Pentoxifylline", "product_id": "70954-668_9732cf08-dad4-42a4-a10e-0284848724d7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Blood Viscosity Reducer [EPC]", "Hematologic Activity Alteration [PE]"], "product_ndc": "70954-668", "generic_name": "Pentoxifylline", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pentoxifylline", "active_ingredients": [{"name": "PENTOXIFYLLINE", "strength": "400 mg/1"}], "application_number": "ANDA074878", "marketing_category": "ANDA", "marketing_start_date": "20240115", "listing_expiration_date": "20261231"}