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United States · US · US:72162-1735_8c615600-bebe-4c68-8803-8100d5260676

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 · 7

  • ndc11
    7216217351
    120 TABLET in 1 BOTTLE, PLASTIC (72162-1735-1)
  • ndc11
    7216217352
    20 TABLET in 1 BOTTLE, PLASTIC (72162-1735-2)
  • ndc11
    7216217353
    30 TABLET in 1 BOTTLE, PLASTIC (72162-1735-3)
  • ndc11
    7216217354
    28 TABLET in 1 BOTTLE, PLASTIC (72162-1735-4)
  • ndc11
    7216217355
    10 TABLET in 1 BOTTLE, PLASTIC (72162-1735-5)
  • ndc11
    7216217356
    60 TABLET in 1 BOTTLE, PLASTIC (72162-1735-6)
  • ndc11
    7216217357
    50 TABLET in 1 BOTTLE, PLASTIC (72162-1735-7)

Annotations

UNII (FDA Substance ID)
X4HES1O11F
ACYCLOVIR
RxCUI 281
Orange Book
A075382
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": "72162-1735_8c615600-bebe-4c68-8803-8100d5260676",
  "productndc": "72162-1735",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "075382",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "001",
        "approval_date": "Apr 30, 1999"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "800MG",
        "product_no": "002",
        "approval_date": "Apr 30, 1999"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ACYCLOVIR",
  "proprietary_name": "Acyclovir",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075382",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Acyclovir",
  "start_marketing_date": "20091022",
  "active_numerator_strength": "400"
}

Related drugs

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