Package 50090-6918-0
Brand: valacyclovir hydrochloride
Generic: valacyclovir hydrochloridePackage Facts
Identity
Package NDC
50090-6918-0
Digits Only
5009069180
Product NDC
50090-6918
Description
90 TABLET, FILM COATED in 1 BOTTLE (50090-6918-0)
Marketing
Marketing Status
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": "09b3c027-4957-4f0b-82e9-1cb50b76c87c", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["87ec59e3-c06a-4ca7-bc65-5b251263ab3b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6918-0)", "package_ndc": "50090-6918-0", "marketing_start_date": "20231213"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "50090-6918_09b3c027-4957-4f0b-82e9-1cb50b76c87c", "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": "50090-6918", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir Hydrochloride", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA090682", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20261231"}