valacyclovir hydrochloride
Generic: valacyclovir hydrochloride
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
valacyclovir hydrochloride
Generic Name
valacyclovir hydrochloride
Labeler
proficient rx lp
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
valacyclovir hydrochloride 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-093
Product ID
82804-093_8333bcde-7bec-4c7e-98f2-ebb5c8eadfd7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090682
Listing Expiration
2027-12-31
Marketing Start
2010-05-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804093
Hyphenated Format
82804-093
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 hydrochloride (source: ndc)
Generic Name
valacyclovir hydrochloride (source: ndc)
Application Number
ANDA090682 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 TABLET, FILM COATED in 1 BOTTLE (82804-093-10)
- 14 TABLET, FILM COATED in 1 BOTTLE (82804-093-14)
- 21 TABLET, FILM COATED in 1 BOTTLE (82804-093-21)
- 30 TABLET, FILM COATED in 1 BOTTLE (82804-093-30)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8333bcde-7bec-4c7e-98f2-ebb5c8eadfd7", "openfda": {"upc": ["0382804093304"], "unii": ["G447S0T1VC"], "rxcui": ["313564"], "spl_set_id": ["fb875f07-e9a0-48eb-a8b0-16ea7bbae9ab"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (82804-093-10)", "package_ndc": "82804-093-10", "marketing_start_date": "20240719"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (82804-093-14)", "package_ndc": "82804-093-14", "marketing_start_date": "20260113"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (82804-093-21)", "package_ndc": "82804-093-21", "marketing_start_date": "20240405"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-093-30)", "package_ndc": "82804-093-30", "marketing_start_date": "20240402"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "82804-093_8333bcde-7bec-4c7e-98f2-ebb5c8eadfd7", "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": "82804-093", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir Hydrochloride", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA090682", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20271231"}