valacyclovir
Generic: valacyclovir
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
valacyclovir
Generic Name
valacyclovir
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
valacyclovir hydrochloride 1000 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-006
Product ID
82804-006_dcd80515-07e5-476c-b923-22bb48af61f3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209553
Listing Expiration
2026-12-31
Marketing Start
2023-02-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804006
Hyphenated Format
82804-006
Supplemental Identifiers
RxCUI
UPC
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
valacyclovir (source: ndc)
Generic Name
valacyclovir (source: ndc)
Application Number
ANDA209553 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
Packaging
- 6 TABLET in 1 BOTTLE (82804-006-06)
- 10 TABLET in 1 BOTTLE (82804-006-10)
- 21 TABLET in 1 BOTTLE (82804-006-21)
- 30 TABLET in 1 BOTTLE (82804-006-30)
- 60 TABLET in 1 BOTTLE (82804-006-60)
- 90 TABLET in 1 BOTTLE (82804-006-90)
Packages (6)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "dcd80515-07e5-476c-b923-22bb48af61f3", "openfda": {"upc": ["0382804006212", "0382804009060"], "unii": ["G447S0T1VC"], "rxcui": ["313564", "313565"], "spl_set_id": ["a3a6a874-f568-429d-96b4-8ef89393564f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (82804-006-06)", "package_ndc": "82804-006-06", "marketing_start_date": "20230908"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (82804-006-10)", "package_ndc": "82804-006-10", "marketing_start_date": "20231226"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (82804-006-21)", "package_ndc": "82804-006-21", "marketing_start_date": "20230908"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-006-30)", "package_ndc": "82804-006-30", "marketing_start_date": "20230908"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-006-60)", "package_ndc": "82804-006-60", "marketing_start_date": "20230908"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-006-90)", "package_ndc": "82804-006-90", "marketing_start_date": "20230908"}], "brand_name": "Valacyclovir", "product_id": "82804-006_dcd80515-07e5-476c-b923-22bb48af61f3", "dosage_form": "TABLET", "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": "82804-006", "generic_name": "Valacyclovir", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA209553", "marketing_category": "ANDA", "marketing_start_date": "20230214", "listing_expiration_date": "20261231"}