Package 60760-757-42

Brand: valacyclovir hydrochloride

Generic: valacyclovir hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-757-42
Digits Only 6076075742
Product NDC 60760-757
Description

42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-757-42)

Marketing

Marketing Status
Marketed Since 2024-11-14
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": "275c0198-10a6-139e-e063-6394a90a72be", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313564"], "spl_set_id": ["275c0198-10a5-139e-e063-6394a90a72be"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-757-42)", "package_ndc": "60760-757-42", "marketing_start_date": "20241114"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "60760-757_275c0198-10a6-139e-e063-6394a90a72be", "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": "60760-757", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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"}