Package 71335-2586-3

Brand: pentoxifylline

Generic: pentoxifylline
NDC Package

Package Facts

Identity

Package NDC 71335-2586-3
Digits Only 7133525863
Product NDC 71335-2586
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-3)

Marketing

Marketing Status
Marketed Since 2025-04-07
Brand pentoxifylline
Generic pentoxifylline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7ee0f77c-2c3e-44fe-9acf-a540e98bd641", "openfda": {"nui": ["N0000175895", "N0000009065"], "unii": ["SD6QCT3TSU"], "rxcui": ["312301"], "spl_set_id": ["c3ad4fb4-8995-46ab-86e9-7ec67ef607f9"], "pharm_class_pe": ["Hematologic Activity Alteration [PE]"], "pharm_class_epc": ["Blood Viscosity Reducer [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-1)", "package_ndc": "71335-2586-1", "marketing_start_date": "20250407"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-2)", "package_ndc": "71335-2586-2", "marketing_start_date": "20250407"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2586-3)", "package_ndc": "71335-2586-3", "marketing_start_date": "20250407"}], "brand_name": "Pentoxifylline", "product_id": "71335-2586_7ee0f77c-2c3e-44fe-9acf-a540e98bd641", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Blood Viscosity Reducer [EPC]", "Hematologic Activity Alteration [PE]"], "product_ndc": "71335-2586", "generic_name": "Pentoxifylline", "labeler_name": "Bryant Ranch Prepack", "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"}