valacyclovir

Generic: valacyclovir

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

Drug Facts

Product Profile

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

valacyclovir hydrochloride 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2510
Product ID 50090-2510_d399bfcb-81d0-4325-abda-9a39216e8529
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203047
Listing Expiration 2027-12-31
Marketing Start 2015-05-25

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 500902510
Hyphenated Format 50090-2510

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 (source: ndc)
Generic Name valacyclovir (source: ndc)
Application Number ANDA203047 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (50090-2510-0)
  • 14 TABLET, FILM COATED in 1 BOTTLE (50090-2510-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-2510-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (50090-2510-3)
source: ndc

Packages (4)

50090-2510-0 10 TABLET, FILM COATED in 1 BOTTLE (50090-2510-0) 50090-2510-1 14 TABLET, FILM COATED in 1 BOTTLE (50090-2510-1) 50090-2510-2 30 TABLET, FILM COATED in 1 BOTTLE (50090-2510-2) 50090-2510-3 90 TABLET, FILM COATED in 1 BOTTLE (50090-2510-3)

Ingredients (1)

valacyclovir hydrochloride (500 mg/1)

Linked Drug Pages (1)

Valacyclovir ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d399bfcb-81d0-4325-abda-9a39216e8529", "openfda": {"unii": ["G447S0T1VC"], "rxcui": ["313564", "313565"], "spl_set_id": ["69301126-c901-4d0d-9acb-91ba1a87cd21"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-2510-0)", "package_ndc": "50090-2510-0", "marketing_start_date": "20150525"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-2510-1)", "package_ndc": "50090-2510-1", "marketing_start_date": "20150525"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-2510-2)", "package_ndc": "50090-2510-2", "marketing_start_date": "20150525"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-2510-3)", "package_ndc": "50090-2510-3", "marketing_start_date": "20180801"}], "brand_name": "Valacyclovir", "product_id": "50090-2510_d399bfcb-81d0-4325-abda-9a39216e8529", "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": "50090-2510", "generic_name": "Valacyclovir", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valacyclovir", "active_ingredients": [{"name": "VALACYCLOVIR HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203047", "marketing_category": "ANDA", "marketing_start_date": "20150525", "listing_expiration_date": "20271231"}