Package 31722-708-60
Brand: famciclovir
Generic: famciclovirPackage Facts
Identity
Package NDC
31722-708-60
Digits Only
3172270860
Product NDC
31722-708
Description
60 TABLET, FILM COATED in 1 BOTTLE (31722-708-60)
Marketing
Marketing Status
Brand
famciclovir
Generic
famciclovir
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b438049-f70c-5388-e063-6394a90af892", "openfda": {"nui": ["N0000020060", "N0000180187", "N0000175459"], "unii": ["QIC03ANI02"], "rxcui": ["198382", "199192", "199193"], "spl_set_id": ["08c58224-5920-4853-8c59-ec5fbb66c2f6"], "pharm_class_epc": ["Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]"], "pharm_class_moa": ["DNA Polymerase Inhibitors [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (31722-708-01)", "package_ndc": "31722-708-01", "marketing_start_date": "20140910"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-708-05)", "package_ndc": "31722-708-05", "marketing_start_date": "20140910"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (31722-708-10)", "package_ndc": "31722-708-10", "marketing_start_date": "20140910"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-708-30)", "package_ndc": "31722-708-30", "marketing_start_date": "20140910"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-708-60)", "package_ndc": "31722-708-60", "marketing_start_date": "20140910"}], "brand_name": "Famciclovir", "product_id": "31722-708_2b438049-f70c-5388-e063-6394a90af892", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["DNA Polymerase Inhibitors [MoA]", "Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "31722-708", "generic_name": "Famciclovir", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famciclovir", "active_ingredients": [{"name": "FAMCICLOVIR", "strength": "500 mg/1"}], "application_number": "ANDA202438", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}