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United States · US · US:71335-1381_ab6cd5b2-f2ba-43b6-99f5-aeedd8a8a069

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
    7133513810
    500 TABLET in 1 BOTTLE (71335-1381-0)
  • ndc11
    7133513811
    25 TABLET in 1 BOTTLE (71335-1381-1)
  • ndc11
    7133513812
    35 TABLET in 1 BOTTLE (71335-1381-2)
  • ndc11
    7133513813
    30 TABLET in 1 BOTTLE (71335-1381-3)
  • ndc11
    7133513814
    60 TABLET in 1 BOTTLE (71335-1381-4)
  • ndc11
    7133513815
    50 TABLET in 1 BOTTLE (71335-1381-5)
  • ndc11
    7133513816
    10 TABLET in 1 BOTTLE (71335-1381-6)
  • ndc11
    7133513817
    40 TABLET in 1 BOTTLE (71335-1381-7)
  • ndc11
    7133513818
    21 TABLET in 1 BOTTLE (71335-1381-8)
  • ndc11
    7133513819
    90 TABLET in 1 BOTTLE (71335-1381-9)

Annotations

UNII (FDA Substance ID)
X4HES1O11F
ACYCLOVIR
RxCUI 281
Orange Book
A077309
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": "71335-1381_ab6cd5b2-f2ba-43b6-99f5-aeedd8a8a069",
  "productndc": "71335-1381",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077309",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "001",
        "approval_date": "Sep 29, 2005"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "800MG",
        "product_no": "002",
        "approval_date": "Sep 29, 2005"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ACYCLOVIR",
  "proprietary_name": "acyclovir",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077309",
  "marketing_category": "ANDA",
  "nonproprietary_name": "acyclovir",
  "start_marketing_date": "20060313",
  "active_numerator_strength": "800"
}

Related drugs

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