valacyclovir hydrochloride

Generic: valacyclovir hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valacyclovir hydrochloride
Generic Name valacyclovir hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valacyclovir hydrochloride 1 g/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1173
Product ID 50090-1173_b776ccd0-5894-416d-879e-0d7ca6f6cfd9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090682
Listing Expiration 2026-12-31
Marketing Start 2010-05-24

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901173
Hyphenated Format 50090-1173

Supplemental Identifiers

RxCUI
313564
UNII
G447S0T1VC

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BOTTLE (50090-1173-0)
  • 21 TABLET, FILM COATED in 1 BOTTLE (50090-1173-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-1173-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-1173-3)
source: ndc

Packages (4)

50090-1173-0 15 TABLET, FILM COATED in 1 BOTTLE (50090-1173-0) 50090-1173-1 21 TABLET, FILM COATED in 1 BOTTLE (50090-1173-1) 50090-1173-2 30 TABLET, FILM COATED in 1 BOTTLE (50090-1173-2) 50090-1173-3 90 TABLET, FILM COATED in 1 BOTTLE (50090-1173-3)

Ingredients (1)

valacyclovir hydrochloride (1 g/1)

Linked Drug Pages (1)

Valacyclovir Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b776ccd0-5894-416d-879e-0d7ca6f6cfd9", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313564"], "spl_set_id": ["8c0be4f6-2d11-41d4-8f57-4f8db9da60b2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-1173-0)", "package_ndc": "50090-1173-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (50090-1173-1)", "package_ndc": "50090-1173-1", "marketing_start_date": "20141128"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-1173-2)", "package_ndc": "50090-1173-2", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-1173-3)", "package_ndc": "50090-1173-3", "marketing_start_date": "20250516"}], "brand_name": "Valacyclovir Hydrochloride", "product_id": "50090-1173_b776ccd0-5894-416d-879e-0d7ca6f6cfd9", "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": "50090-1173", "generic_name": "Valacyclovir Hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}