Package 67296-1297-1
Brand: valacyclovir
Generic: valacyclovirPackage Facts
Identity
Package NDC
67296-1297-1
Digits Only
6729612971
Product NDC
67296-1297
Description
21 TABLET, FILM COATED in 1 BOTTLE (67296-1297-1)
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": "1d6fdd9f-1ba0-095b-e063-6394a90ac467", "openfda": {"upc": ["0331722704304", "0367296129717", "0331722705301"], "unii": ["G447S0T1VC"], "rxcui": ["313564"], "spl_set_id": ["a5030b9d-1adb-f474-e053-2995a90ae0a0"], "manufacturer_name": ["RedPharm Drug, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (67296-1297-1)", "package_ndc": "67296-1297-1", "marketing_start_date": "20150525"}], "brand_name": "Valacyclovir", "product_id": "67296-1297_1d6fdd9f-1ba0-095b-e063-6394a90ac467", "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": "67296-1297", "generic_name": "Valacyclovir", "labeler_name": "RedPharm Drug, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA203047", "marketing_category": "ANDA", "marketing_start_date": "20150525", "listing_expiration_date": "20261231"}