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United States · US · US:71335-3103_465aaa54-8e0b-4a0e-9ea0-7f01ba2a6152

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
    7133531030
    120 TABLET in 1 BOTTLE (71335-3103-0)
  • ndc11
    7133531031
    20 TABLET in 1 BOTTLE (71335-3103-1)
  • ndc11
    7133531032
    28 TABLET in 1 BOTTLE (71335-3103-2)
  • ndc11
    7133531033
    30 TABLET in 1 BOTTLE (71335-3103-3)
  • ndc11
    7133531034
    50 TABLET in 1 BOTTLE (71335-3103-4)
  • ndc11
    7133531035
    15 TABLET in 1 BOTTLE (71335-3103-5)
  • ndc11
    7133531036
    60 TABLET in 1 BOTTLE (71335-3103-6)
  • ndc11
    7133531037
    25 TABLET in 1 BOTTLE (71335-3103-7)
  • ndc11
    7133531038
    10 TABLET in 1 BOTTLE (71335-3103-8)
  • ndc11
    7133531039
    40 TABLET in 1 BOTTLE (71335-3103-9)

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": "71335-3103_465aaa54-8e0b-4a0e-9ea0-7f01ba2a6152",
  "productndc": "71335-3103",
  "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": "20230620",
  "active_numerator_strength": "400"
}

Related drugs

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