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United States · US · US:36000-362_74192a42-0ff7-443b-9d8a-3096ef5c8e43

phenylephrine hydrochloride

Orange BookUNIISPLATC R01AA04

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

Identification

ManufacturerBaxter Healthcare Corporation
CountryUS (United States)
ATC codeR01AA04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    3600036205
    5 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (36000-362-05) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE

Annotations

UNII (FDA Substance ID)
04JA59TNSJ
PHENYLEPHRINE HYDROCHLORIDE
RxCUI 8164
Orange Book
A217032
AP1AP1AP1
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "04JA59TNSJ",
    "rxcui": "8164",
    "inchikey": "OCYSGIYOVXAGKQ-FVGYRXGTSA-N",
    "display_name": "PHENYLEPHRINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "d92631a6-bae8-493b-b4df-c563346607a8": {
      "match": "brand_token",
      "title": "PHENYLEPHRINE HYDROCHLORIDE INJECTION [PAR HEALTH USA, LLC]",
      "spl_version": "15",
      "published_date": "2026-05-20"
    }
  },
  "productid": "36000-362_74192a42-0ff7-443b-9d8a-3096ef5c8e43",
  "productndc": "36000-362",
  "dosage_form": "INJECTION",
  "orange_book": {
    "appl_no": "217032",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AP1",
        "strength": "10MG/ML (10MG/ML)",
        "product_no": "001",
        "approval_date": "Apr 3, 2026"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AP1",
        "strength": "50MG/5ML (10MG/ML)",
        "product_no": "002",
        "approval_date": "Apr 3, 2026"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AP1",
        "strength": "100MG/10ML (10MG/ML)",
        "product_no": "003",
        "approval_date": "Apr 3, 2026"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PHENYLEPHRINE HYDROCHLORIDE",
  "proprietary_name": "phenylephrine hydrochloride",
  "active_ingred_unit": "mg/mL",
  "application_number": "ANDA217032",
  "marketing_category": "ANDA",
  "nonproprietary_name": "phenylephrine hydrochloride",
  "start_marketing_date": "20260406",
  "active_numerator_strength": "10"
}

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