valacyclovir hydrochloride
Generic: valacyclovir hydrochloride
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
valacyclovir hydrochloride
Generic Name
valacyclovir hydrochloride
Labeler
asclemed usa, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
valacyclovir hydrochloride 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
76420-600
Product ID
76420-600_1cf37738-8be1-f5cf-e063-6394a90af194
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090682
Listing Expiration
2026-12-31
Marketing Start
2010-05-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420600
Hyphenated Format
76420-600
Supplemental Identifiers
RxCUI
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
- 2 TABLET, FILM COATED in 1 BOTTLE (76420-600-02)
- 4 TABLET, FILM COATED in 1 BOTTLE (76420-600-04)
- 7 TABLET, FILM COATED in 1 BOTTLE (76420-600-07)
- 10 TABLET, FILM COATED in 1 BOTTLE (76420-600-10)
- 15 TABLET, FILM COATED in 1 BOTTLE (76420-600-15)
- 20 TABLET, FILM COATED in 1 BOTTLE (76420-600-20)
- 21 TABLET, FILM COATED in 1 BOTTLE (76420-600-21)
- 30 TABLET, FILM COATED in 1 BOTTLE (76420-600-30)
Packages (8)
76420-600-02
2 TABLET, FILM COATED in 1 BOTTLE (76420-600-02)
76420-600-04
4 TABLET, FILM COATED in 1 BOTTLE (76420-600-04)
76420-600-07
7 TABLET, FILM COATED in 1 BOTTLE (76420-600-07)
76420-600-10
10 TABLET, FILM COATED in 1 BOTTLE (76420-600-10)
76420-600-15
15 TABLET, FILM COATED in 1 BOTTLE (76420-600-15)
76420-600-20
20 TABLET, FILM COATED in 1 BOTTLE (76420-600-20)
76420-600-21
21 TABLET, FILM COATED in 1 BOTTLE (76420-600-21)
76420-600-30
30 TABLET, FILM COATED in 1 BOTTLE (76420-600-30)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1cf37738-8be1-f5cf-e063-6394a90af194", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313564"], "spl_set_id": ["1864bf8b-07a2-4b82-8592-bf8ad6f9f8f9"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (76420-600-02)", "package_ndc": "76420-600-02", "marketing_start_date": "20230906"}, {"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (76420-600-04)", "package_ndc": "76420-600-04", "marketing_start_date": "20230906"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (76420-600-07)", "package_ndc": "76420-600-07", "marketing_start_date": "20230906"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (76420-600-10)", "package_ndc": "76420-600-10", "marketing_start_date": "20230906"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (76420-600-15)", "package_ndc": "76420-600-15", "marketing_start_date": "20230906"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (76420-600-20)", "package_ndc": "76420-600-20", "marketing_start_date": "20230906"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (76420-600-21)", "package_ndc": "76420-600-21", "marketing_start_date": "20240711"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-600-30)", "package_ndc": "76420-600-30", "marketing_start_date": "20230906"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "76420-600_1cf37738-8be1-f5cf-e063-6394a90af194", "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": "76420-600", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "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": "20261231"}