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United States · US · US:71335-1222_af2a25d9-8333-4f9e-8ff8-36562f8d654f

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
    7133512220
    500 TABLET in 1 BOTTLE (71335-1222-0)
  • ndc11
    7133512221
    25 TABLET in 1 BOTTLE (71335-1222-1)
  • ndc11
    7133512222
    35 TABLET in 1 BOTTLE (71335-1222-2)
  • ndc11
    7133512223
    30 TABLET in 1 BOTTLE (71335-1222-3)
  • ndc11
    7133512224
    60 TABLET in 1 BOTTLE (71335-1222-4)
  • ndc11
    7133512225
    50 TABLET in 1 BOTTLE (71335-1222-5)
  • ndc11
    7133512226
    10 TABLET in 1 BOTTLE (71335-1222-6)
  • ndc11
    7133512227
    40 TABLET in 1 BOTTLE (71335-1222-7)
  • ndc11
    7133512228
    21 TABLET in 1 BOTTLE (71335-1222-8)
  • ndc11
    7133512229
    90 TABLET in 1 BOTTLE (71335-1222-9)

Annotations

UNII (FDA Substance ID)
X4HES1O11F
ACYCLOVIR
RxCUI 281
Orange Book
A210401
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": "71335-1222_af2a25d9-8333-4f9e-8ff8-36562f8d654f",
  "productndc": "71335-1222",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "210401",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "001",
        "approval_date": "Mar 7, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "800MG",
        "product_no": "002",
        "approval_date": "Mar 7, 2018"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ACYCLOVIR",
  "proprietary_name": "Acyclovir",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA210401",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Acyclovir",
  "start_marketing_date": "20180504",
  "active_numerator_strength": "800"
}

Related drugs

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