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United States · US · US:71335-2555_904c860d-4d2e-4360-ab30-4242e43d379e

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
    7133525550
    500 TABLET in 1 BOTTLE (71335-2555-0)
  • ndc11
    7133525551
    25 TABLET in 1 BOTTLE (71335-2555-1)
  • ndc11
    7133525552
    35 TABLET in 1 BOTTLE (71335-2555-2)
  • ndc11
    7133525553
    30 TABLET in 1 BOTTLE (71335-2555-3)
  • ndc11
    7133525554
    60 TABLET in 1 BOTTLE (71335-2555-4)
  • ndc11
    7133525555
    50 TABLET in 1 BOTTLE (71335-2555-5)
  • ndc11
    7133525556
    10 TABLET in 1 BOTTLE (71335-2555-6)
  • ndc11
    7133525557
    40 TABLET in 1 BOTTLE (71335-2555-7)
  • ndc11
    7133525558
    21 TABLET in 1 BOTTLE (71335-2555-8)
  • ndc11
    7133525559
    90 TABLET in 1 BOTTLE (71335-2555-9)

Annotations

UNII (FDA Substance ID)
X4HES1O11F
ACYCLOVIR
RxCUI 281
Orange Book
A209366
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": "71335-2555_904c860d-4d2e-4360-ab30-4242e43d379e",
  "productndc": "71335-2555",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "209366",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "001",
        "approval_date": "Oct 7, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "800MG",
        "product_no": "002",
        "approval_date": "Oct 7, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ACYCLOVIR",
  "proprietary_name": "Acyclovir",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA209366",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Acyclovir",
  "start_marketing_date": "20200815",
  "active_numerator_strength": "800"
}

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