Package 82868-055-21
Brand: valacyclovir hydrochloride
Generic: valacyclovirPackage Facts
Identity
Package NDC
82868-055-21
Digits Only
8286805521
Product NDC
82868-055
Description
21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-055-21)
Marketing
Marketing Status
Brand
valacyclovir hydrochloride
Generic
valacyclovir
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46dcc5db-2924-de8f-e063-6394a90a101f", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["1b53c6bb-0e8c-f49a-e063-6294a90a0f5a"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-055-21)", "package_ndc": "82868-055-21", "marketing_start_date": "20240530"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "82868-055_46dcc5db-2924-de8f-e063-6394a90a101f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["DNA Polymerase Inhibitors [MoA]", "Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "82868-055", "generic_name": "valacyclovir", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir Hydrochloride", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078518", "marketing_category": "ANDA", "marketing_start_date": "20240530", "listing_expiration_date": "20261231"}