Package 72789-263-14

Brand: valacyclovir hydrochloride

Generic: valacyclovir hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-263-14
Digits Only 7278926314
Product NDC 72789-263
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-14)

Marketing

Marketing Status
Marketed Since 2023-12-04
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": "4bace031-383a-f25c-e063-6294a90a27da", "openfda": {"upc": ["0372789263281"], "unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["ae8d15a4-1ed5-4e3c-9672-0f4735322a1c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-06)", "package_ndc": "72789-263-06", "marketing_start_date": "20250618"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-10)", "package_ndc": "72789-263-10", "marketing_start_date": "20221011"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-14)", "package_ndc": "72789-263-14", "marketing_start_date": "20231204"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-28)", "package_ndc": "72789-263-28", "marketing_start_date": "20250303"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-90)", "package_ndc": "72789-263-90", "marketing_start_date": "20220720"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "72789-263_4bace031-383a-f25c-e063-6294a90a27da", "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": "72789-263", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20271231"}