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United States · US · US:0615-8511_e3966eca-d995-479b-b2a3-4fd6eea51cb1

Pentoxifylline

Orange BookUNIISPLATC C04AD03

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
CountryUS (United States)
ATC codeC04AD03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0615851139
    30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8511-39)

Annotations

UNII (FDA Substance ID)
SD6QCT3TSU
PENTOXIFYLLINE
RxCUI 8013
Orange Book
A074878
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "SD6QCT3TSU",
    "rxcui": "8013",
    "inchikey": "BYPFEZZEUUWMEJ-UHFFFAOYSA-N",
    "display_name": "PENTOXIFYLLINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "08b095b6-be53-41f5-a284-fe15d4852f79": {
      "match": "brand_token",
      "title": "PENTOXIFYLLINE POWDER [AX PHARMACEUTICAL CORP]",
      "spl_version": "3",
      "published_date": "2026-03-12"
    }
  },
  "productid": "0615-8511_e3966eca-d995-479b-b2a3-4fd6eea51cb1",
  "productndc": "0615-8511",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "074878",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "400MG",
        "product_no": "001",
        "approval_date": "Jul 9, 1997"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PENTOXIFYLLINE",
  "proprietary_name": "Pentoxifylline",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA074878",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Pentoxifylline",
  "start_marketing_date": "20240115",
  "active_numerator_strength": "400"
}

Related drugs

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