Package 68071-3749-4
Brand: valacyclovir
Generic: valacyclovirPackage Facts
Identity
Package NDC
68071-3749-4
Digits Only
6807137494
Product NDC
68071-3749
Description
14 TABLET, FILM COATED in 1 BOTTLE (68071-3749-4)
Marketing
Marketing Status
Brand
valacyclovir
Generic
valacyclovir
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a09600d-c2fa-0a52-e063-6394a90a228c", "openfda": {"upc": ["0368071374940"], "unii": ["G447S0T1VC"], "rxcui": ["313565"], "spl_set_id": ["29a6b4ec-3e23-289b-e063-6394a90a1157"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68071-3749-4)", "package_ndc": "68071-3749-4", "marketing_start_date": "20241219"}], "brand_name": "Valacyclovir", "product_id": "68071-3749_2a09600d-c2fa-0a52-e063-6394a90a228c", "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": "68071-3749", "generic_name": "Valacyclovir", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203047", "marketing_category": "ANDA", "marketing_start_date": "20150525", "listing_expiration_date": "20261231"}