Package 67296-2127-2

Brand: valacyclovir hydrochloride

Generic: valacyclovir
NDC Package

Package Facts

Identity

Package NDC 67296-2127-2
Digits Only 6729621272
Product NDC 67296-2127
Description

21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67296-2127-2)

Marketing

Marketing Status
Marketed Since 2010-05-24
Brand valacyclovir hydrochloride
Generic valacyclovir
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4698c788-aa02-6afb-e063-6394a90a708e", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["301edb6c-9ce0-f9fa-e063-6294a90a2909"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67296-2127-2)", "package_ndc": "67296-2127-2", "marketing_start_date": "20100524"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "67296-2127_4698c788-aa02-6afb-e063-6394a90a708e", "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": "67296-2127", "generic_name": "valacyclovir", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir Hydrochloride", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA078518", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20261231"}