Package 60505-0033-7

Brand: pentoxifylline

Generic: pentoxifylline
NDC Package

Package Facts

Identity

Package NDC 60505-0033-7
Digits Only 6050500337
Product NDC 60505-0033
Product ID 60505-0033_e67bdb49-8c37-8b4f-c982-67d024d3f2aa
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-0033-7)

Marketing

Marketing Status
Marketed Since 1999-06-10
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": "e67bdb49-8c37-8b4f-c982-67d024d3f2aa", "openfda": {"nui": ["N0000175895", "N0000009065"], "unii": ["SD6QCT3TSU"], "rxcui": ["312301"], "spl_set_id": ["40ae2d9a-0d95-640d-0640-f76e7e1a13cb"], "pharm_class_pe": ["Hematologic Activity Alteration [PE]"], "pharm_class_epc": ["Blood Viscosity Reducer [EPC]"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-0033-6)", "package_ndc": "60505-0033-6", "marketing_start_date": "19990610"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-0033-7)", "package_ndc": "60505-0033-7", "marketing_start_date": "19990610"}], "brand_name": "PENTOXIFYLLINE", "product_id": "60505-0033_e67bdb49-8c37-8b4f-c982-67d024d3f2aa", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Blood Viscosity Reducer [EPC]", "Hematologic Activity Alteration [PE]"], "product_ndc": "60505-0033", "generic_name": "PENTOXIFYLLINE", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PENTOXIFYLLINE", "active_ingredients": [{"name": "PENTOXIFYLLINE", "strength": "400 mg/1"}], "application_number": "ANDA075191", "marketing_category": "ANDA", "marketing_start_date": "19990610", "listing_expiration_date": "20261231"}