Package 16714-698-03

Brand: valacyclovir hydrochloride

Generic: valacyclovir hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-698-03
Digits Only 1671469803
Product NDC 16714-698
Description

90 TABLET, FILM COATED in 1 BOTTLE (16714-698-03)

Marketing

Marketing Status
Marketed Since 2010-05-24
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": "086d34eb-21bb-4159-80c3-8e64eda1b6e5", "openfda": {"upc": ["0316714697031"], "unii": ["G447S0T1VC"], "rxcui": ["313564", "313565"], "spl_set_id": ["4acf51de-26f7-42b2-8acc-61b800627ef3"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (16714-698-03)", "package_ndc": "16714-698-03", "marketing_start_date": "20100524"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "16714-698_086d34eb-21bb-4159-80c3-8e64eda1b6e5", "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": "16714-698", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "NorthStar Rx LLC", "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"}