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United States · US · US:0703-0686_c7be0baa-694d-498d-a474-3611f7773954

Treprostinil

Orange BookUNIISPLATC B01AC21

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

Identification

ManufacturerTeva Parenteral Medicines, Inc.
CountryUS (United States)
ATC codeB01AC21
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0703068601
    1 VIAL, MULTI-DOSE in 1 CARTON (0703-0686-01) / 20 mL in 1 VIAL, MULTI-DOSE

Annotations

UNII (FDA Substance ID)
RUM6K67ESG
TREPROSTINIL
RxCUI 343048
Orange Book
A206648
APAPAPAP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "RUM6K67ESG",
    "rxcui": "343048",
    "inchikey": "PAJMKGZZBBTTOY-ZFORQUDYSA-N",
    "display_name": "TREPROSTINIL",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS; SUBCUTANEOUS",
  "spl_meta": {
    "4a684b13-669d-4721-8ed4-30cc7762b0b8": {
      "match": "brand_token",
      "title": "TREPROSTINIL INJECTION, SOLUTION [ALEMBIC PHARMACEUTICALS INC.]",
      "spl_version": "8",
      "published_date": "2025-03-13"
    }
  },
  "productid": "0703-0686_c7be0baa-694d-498d-a474-3611f7773954",
  "productndc": "0703-0686",
  "dosage_form": "INJECTION, SOLUTION",
  "orange_book": {
    "appl_no": "206648",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "1MG/ML",
        "product_no": "001",
        "approval_date": "Sep 26, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "2.5MG/ML",
        "product_no": "002",
        "approval_date": "Sep 26, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "5MG/ML",
        "product_no": "003",
        "approval_date": "Sep 26, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AP",
        "strength": "10MG/ML",
        "product_no": "004",
        "approval_date": "Sep 26, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "TREPROSTINIL",
  "proprietary_name": "Treprostinil",
  "active_ingred_unit": "mg/20mL",
  "application_number": "ANDA206648",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Treprostinil",
  "start_marketing_date": "20190930",
  "active_numerator_strength": "100"
}

Related drugs

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