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United States · US · US:70594-063_69ee5794-96b0-4975-aadd-d8dbcc73ca3f

Phenylephrine Hydrochloride

Orange BookUNIISPLATC R01AA04

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

Identification

ManufacturerXellia Pharmaceuticals USA LLC
CountryUS (United States)
ATC codeR01AA04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7059406302
    25 VIAL in 1 CARTON (70594-063-02) / 1 mL in 1 VIAL (70594-063-01)

Annotations

UNII (FDA Substance ID)
04JA59TNSJ
PHENYLEPHRINE HYDROCHLORIDE
RxCUI 8164
Orange Book
A213318
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": "70594-063_69ee5794-96b0-4975-aadd-d8dbcc73ca3f",
  "productndc": "70594-063",
  "dosage_form": "INJECTION",
  "orange_book": {
    "appl_no": "213318",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AP1",
        "strength": "10MG/ML (10MG/ML)",
        "product_no": "001",
        "approval_date": "Jun 11, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AP1",
        "strength": "50MG/5ML (10MG/ML)",
        "product_no": "002",
        "approval_date": "Jun 11, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AP1",
        "strength": "100MG/10ML (10MG/ML)",
        "product_no": "003",
        "approval_date": "Jun 11, 2020"
      }
    ],
    "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": "ANDA213318",
  "marketing_category": "ANDA",
  "nonproprietary_name": "PHENYLEPHRINE HYDROCHLORIDE",
  "start_marketing_date": "20220101",
  "active_numerator_strength": "10"
}

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