Package 64980-350-03

Brand: famciclovir

Generic: famciclovir
NDC Package

Package Facts

Identity

Package NDC 64980-350-03
Digits Only 6498035003
Product NDC 64980-350
Product ID 64980-350_edd6ee53-72b7-48e5-aef4-30c077db7545
Description

30 TABLET, FILM COATED in 1 BOTTLE (64980-350-03)

Marketing

Marketing Status
Marketed Since 2011-03-21
Brand famciclovir
Generic famciclovir
Sample Package No

Linked Drug Pages (1)

Famciclovir ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "edd6ee53-72b7-48e5-aef4-30c077db7545", "openfda": {"nui": ["N0000020060", "N0000180187", "N0000175459"], "unii": ["QIC03ANI02"], "rxcui": ["198382", "199192", "199193"], "spl_set_id": ["d5c46506-a350-44a1-9440-d939da895f16"], "pharm_class_epc": ["Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]"], "pharm_class_moa": ["DNA Polymerase Inhibitors [MoA]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (64980-350-03)", "package_ndc": "64980-350-03", "marketing_start_date": "20110321"}], "brand_name": "Famciclovir", "product_id": "64980-350_edd6ee53-72b7-48e5-aef4-30c077db7545", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["DNA Polymerase Inhibitors [MoA]", "Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "64980-350", "generic_name": "Famciclovir", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famciclovir", "active_ingredients": [{"name": "FAMCICLOVIR", "strength": "250 mg/1"}], "application_number": "ANDA091114", "marketing_category": "ANDA", "marketing_start_date": "20110321", "listing_expiration_date": "20261231"}