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United States · US · US:65862-448_aecf12c1-9094-48b6-8cb0-fcace52e191a

Valacyclovir Hydrochloride

Orange BookUNIISPLATC J05AB11

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAurobindo Pharma Limited
CountryUS (United States)
ATC codeJ05AB11
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    6586244801
    100 TABLET, FILM COATED in 1 BOTTLE (65862-448-01)
  • ndc11
    6586244805
    500 TABLET, FILM COATED in 1 BOTTLE (65862-448-05)
  • ndc11
    6586244810
    10 BLISTER PACK in 1 CARTON (65862-448-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    6586244830
    30 TABLET, FILM COATED in 1 BOTTLE (65862-448-30)
  • ndc11
    6586244835
    3500 TABLET, FILM COATED in 1 BOTTLE (65862-448-35)
  • ndc11
    6586244890
    90 TABLET, FILM COATED in 1 BOTTLE (65862-448-90)

Annotations

UNII (FDA Substance ID)
G447S0T1VC
VALACYCLOVIR HYDROCHLORIDE
RxCUI 236081
Orange Book
A090682
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "G447S0T1VC",
    "rxcui": "236081",
    "inchikey": "ZCDDBUOENGJMLV-QRPNPIFTSA-N",
    "display_name": "VALACYCLOVIR HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "021ab9d0-7b75-40cf-afde-446942d64388": {
      "match": "brand_token",
      "title": "VALACYCLOVIR HYDROCHLORIDE (VALACYCLOVIR) TABLET, FILM COATED [SAFECOR HEALTH LLC]",
      "spl_version": "3",
      "published_date": "2026-06-01"
    }
  },
  "productid": "65862-448_aecf12c1-9094-48b6-8cb0-fcace52e191a",
  "productndc": "65862-448",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "090682",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 500MG BASE",
        "product_no": "001",
        "approval_date": "May 24, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 1GM BASE",
        "product_no": "002",
        "approval_date": "May 24, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "VALACYCLOVIR HYDROCHLORIDE",
  "proprietary_name": "Valacyclovir Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090682",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Valacyclovir Hydrochloride",
  "start_marketing_date": "20100524",
  "active_numerator_strength": "500"
}

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