Package 50090-7484-0

Brand: valacyclovir

Generic: valacyclovir
NDC Package

Package Facts

Identity

Package NDC 50090-7484-0
Digits Only 5009074840
Product NDC 50090-7484
Product ID 50090-7484_88a543ff-245b-4486-9464-5d8a66d741cd
Description

21 TABLET in 1 BOTTLE (50090-7484-0)

Marketing

Marketing Status
Marketed Since 2024-12-20
Brand valacyclovir
Generic valacyclovir
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "88a543ff-245b-4486-9464-5d8a66d741cd", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313564"], "spl_set_id": ["5af8f909-ad53-480e-9176-43f95dcc218a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (50090-7484-0)", "package_ndc": "50090-7484-0", "marketing_start_date": "20241220"}], "brand_name": "Valacyclovir", "product_id": "50090-7484_88a543ff-245b-4486-9464-5d8a66d741cd", "dosage_form": "TABLET", "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": "50090-7484", "generic_name": "Valacyclovir", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA209553", "marketing_category": "ANDA", "marketing_start_date": "20230214", "listing_expiration_date": "20261231"}