Package 65862-449-05

Brand: valacyclovir hydrochloride

Generic: valacyclovir hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65862-449-05
Digits Only 6586244905
Product NDC 65862-449
Description

500 TABLET, FILM COATED in 1 BOTTLE (65862-449-05)

Marketing

Marketing Status
Marketed Since 2010-05-24
Brand valacyclovir hydrochloride
Generic valacyclovir hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aecf12c1-9094-48b6-8cb0-fcace52e191a", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313564", "313565"], "spl_set_id": ["f5cfb61e-d971-4a9c-b9ef-4f3368fe02f5"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-449-01)", "package_ndc": "65862-449-01", "marketing_start_date": "20100524"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-449-05)", "package_ndc": "65862-449-05", "marketing_start_date": "20100524"}, {"sample": false, "description": "1500 TABLET, FILM COATED in 1 BOTTLE (65862-449-15)", "package_ndc": "65862-449-15", "marketing_start_date": "20100524"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-449-30)", "package_ndc": "65862-449-30", "marketing_start_date": "20100524"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-449-90)", "package_ndc": "65862-449-90", "marketing_start_date": "20100524"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "65862-449_aecf12c1-9094-48b6-8cb0-fcace52e191a", "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": "65862-449", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir Hydrochloride", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA090682", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20261231"}