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
Routes
ORAL
Active Ingredients

valacyclovir hydrochloride 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1735
Product ID 50090-1735_40bb864c-a964-4b3d-8613-977890d4326a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077135
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 500901735
Hyphenated Format 50090-1735

Supplemental Identifiers

RxCUI
313564 313565
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 ANDA077135 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (50090-1735-0)
  • 14 TABLET in 1 BOTTLE (50090-1735-1)
  • 30 TABLET in 1 BOTTLE (50090-1735-2)
  • 90 TABLET in 1 BOTTLE (50090-1735-3)
source: ndc

Packages (4)

50090-1735-0 10 TABLET in 1 BOTTLE (50090-1735-0) 50090-1735-1 14 TABLET in 1 BOTTLE (50090-1735-1) 50090-1735-2 30 TABLET in 1 BOTTLE (50090-1735-2) 50090-1735-3 90 TABLET in 1 BOTTLE (50090-1735-3)

Ingredients (1)

valacyclovir hydrochloride (500 mg/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": "40bb864c-a964-4b3d-8613-977890d4326a", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313564", "313565"], "spl_set_id": ["cb929bed-0e7d-4543-9020-edfda93d78fc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (50090-1735-0)", "package_ndc": "50090-1735-0", "marketing_start_date": "20150310"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-1735-1)", "package_ndc": "50090-1735-1", "marketing_start_date": "20150310"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1735-2)", "package_ndc": "50090-1735-2", "marketing_start_date": "20150310"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-1735-3)", "package_ndc": "50090-1735-3", "marketing_start_date": "20170503"}], "brand_name": "Valacyclovir hydrochloride", "product_id": "50090-1735_40bb864c-a964-4b3d-8613-977890d4326a", "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": "50090-1735", "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": "500 mg/1"}], "application_number": "ANDA077135", "marketing_category": "ANDA", "marketing_start_date": "20100524", "listing_expiration_date": "20261231"}