Package 70518-4417-0
Brand: valacyclovir
Generic: valacyclovirPackage Facts
Identity
Package NDC
70518-4417-0
Digits Only
7051844170
Product NDC
70518-4417
Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4417-0)
Marketing
Marketing Status
Brand
valacyclovir
Generic
valacyclovir
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b8c10f7-2708-6dde-e063-6294a90af835", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["2c2d5cec-038f-42bb-8f04-90d2431dc1c9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4417-0)", "package_ndc": "70518-4417-0", "marketing_start_date": "20250731"}], "brand_name": "Valacyclovir", "product_id": "70518-4417_3b8c10f7-2708-6dde-e063-6294a90af835", "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": "70518-4417", "generic_name": "Valacyclovir", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203047", "marketing_category": "ANDA", "marketing_start_date": "20250731", "listing_expiration_date": "20261231"}