Package 68071-4532-9

Brand: pentoxifylline

Generic: pentoxifylline
NDC Package

Package Facts

Identity

Package NDC 68071-4532-9
Digits Only 6807145329
Product NDC 68071-4532
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4532-9)

Marketing

Marketing Status
Marketed Since 2018-08-17
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": "1a909abe-99ac-0b35-e063-6394a90aac4a", "openfda": {"nui": ["N0000175895", "N0000009065"], "upc": ["0368071453294"], "unii": ["SD6QCT3TSU"], "rxcui": ["312301"], "spl_set_id": ["73a6351c-5a8d-abbf-e053-2991aa0a5382"], "pharm_class_pe": ["Hematologic Activity Alteration [PE]"], "pharm_class_epc": ["Blood Viscosity Reducer [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4532-9)", "package_ndc": "68071-4532-9", "marketing_start_date": "20180817"}], "brand_name": "Pentoxifylline", "product_id": "68071-4532_1a909abe-99ac-0b35-e063-6394a90aac4a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Blood Viscosity Reducer [EPC]", "Hematologic Activity Alteration [PE]"], "product_ndc": "68071-4532", "generic_name": "Pentoxifylline", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pentoxifylline", "active_ingredients": [{"name": "PENTOXIFYLLINE", "strength": "400 mg/1"}], "application_number": "ANDA075028", "marketing_category": "ANDA", "marketing_start_date": "20140822", "listing_expiration_date": "20261231"}