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United States · US · US:71335-0323_e20bedec-0eb8-4d24-9148-a3ece431dcba

Acyclovir

Orange BookUNIISPLATC J05AB01

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeJ05AB01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133503230
    120 TABLET in 1 BOTTLE (71335-0323-0)
  • ndc11
    7133503231
    20 TABLET in 1 BOTTLE (71335-0323-1)
  • ndc11
    7133503232
    28 TABLET in 1 BOTTLE (71335-0323-2)
  • ndc11
    7133503233
    30 TABLET in 1 BOTTLE (71335-0323-3)
  • ndc11
    7133503234
    50 TABLET in 1 BOTTLE (71335-0323-4)
  • ndc11
    7133503235
    15 TABLET in 1 BOTTLE (71335-0323-5)
  • ndc11
    7133503236
    60 TABLET in 1 BOTTLE (71335-0323-6)
  • ndc11
    7133503237
    25 TABLET in 1 BOTTLE (71335-0323-7)
  • ndc11
    7133503238
    10 TABLET in 1 BOTTLE (71335-0323-8)
  • ndc11
    7133503239
    40 TABLET in 1 BOTTLE (71335-0323-9)

Annotations

UNII (FDA Substance ID)
X4HES1O11F
ACYCLOVIR
RxCUI 281
Orange Book
A203834
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "X4HES1O11F",
    "rxcui": "281",
    "inchikey": "MKUXAQIIEYXACX-UHFFFAOYSA-N",
    "display_name": "ACYCLOVIR",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "db0a0ce5-dc39-4bd3-8b97-21ce9c9999f0": {
      "match": "brand_token",
      "title": "ACYCLOVIR TABLET [PD-RX PHARMACEUTICALS, INC.]",
      "spl_version": "19",
      "published_date": "2026-05-28"
    }
  },
  "productid": "71335-0323_e20bedec-0eb8-4d24-9148-a3ece431dcba",
  "productndc": "71335-0323",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "203834",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "001",
        "approval_date": "Oct 29, 2013"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "800MG",
        "product_no": "002",
        "approval_date": "Oct 29, 2013"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ACYCLOVIR",
  "proprietary_name": "Acyclovir",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA203834",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Acyclovir",
  "start_marketing_date": "20131129",
  "active_numerator_strength": "400"
}

Related drugs

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