(CHLOROPROCAINE HCI

Orange BookUNIISPLATC S01HA08

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHF Acquisition Co LLC, DBA HealthFirst

CountryUS (United States)

ATC codeS01HA08

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
5166214071
30 mL in 1 VIAL, MULTI-DOSE (51662-1407-1)
ndc11
5166214073
25 POUCH in 1 CASE (51662-1407-3) / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1407-2) / 30 mL in 1 VIAL, MULTI-DOSE

Annotations

UNII (FDA Substance ID)

LT7Z1YW11H

CHLOROPROCAINE HYDROCHLORIDE

RxCUI 53616

Orange Book

N009435

APAPAP

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "LT7Z1YW11H",
    "rxcui": "53616",
    "inchikey": "SZKQYDBPUCZLRX-UHFFFAOYSA-N",
    "display_name": "CHLOROPROCAINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INFILTRATION; PERINEURAL",
  "spl_meta": {
    "94d13f48-fbca-67b4-e053-2995a90a791b": {
      "match": "brand_token",
      "title": "(CHLOROPROCAINE HCI INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST]",
      "spl_version": "4",
      "published_date": "2024-01-31"
    }
  },
  "productid": "51662-1407_101e2af0-c51e-edc4-e063-6394a90a8b8c",
  "productndc": "51662-1407",
  "dosage_form": "INJECTION, SOLUTION",
  "orange_book": {
    "appl_no": "009435",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "1%",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AP",
        "strength": "2%",
        "product_no": "002",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "2%",
        "product_no": "003",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "3%",
        "product_no": "004",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AP",
        "strength": "2%",
        "product_no": "006",
        "approval_date": "May 2, 1996"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AP",
        "strength": "3%",
        "product_no": "007",
        "approval_date": "May 2, 1996"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CHLOROPROCAINE HYDROCHLORIDE",
  "proprietary_name": "(CHLOROPROCAINE HCI",
  "active_ingred_unit": "mg/mL",
  "application_number": "NDA009435",
  "marketing_category": "NDA",
  "nonproprietary_name": "(CHLOROPROCAINE HCI",
  "start_marketing_date": "20191013",
  "active_numerator_strength": "10"
}

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