Sodium Chloride

In shortageOrange BookUNIISPLATC A12CA01

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

Identification

ManufacturerHospira, Inc.

CountryUS (United States)

ATC codeA12CA01

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
0409488810
25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)
ndc11
0409488812
25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-12) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-01)
ndc11
0409488820
25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-20) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-4888-03)
ndc11
0409488850
25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-50) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4888-06)
ndc11
0409488890
10 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-90) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)

Annotations

UNII (FDA Substance ID)

451W47IQ8X

SODIUM CHLORIDE

RxCUI 9863

Orange Book

N018803

APAPAP

DailyMed SPL labels

1 version tracked

FDA shortage

Currently in shortage

Sodium Oxybate Solution

Raw payload (JSON)

{
  "unii": {
    "unii": "451W47IQ8X",
    "rxcui": "9863",
    "inchikey": "FAPWRFPIFSIZLT-UHFFFAOYSA-M",
    "display_name": "SODIUM CHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS",
  "spl_meta": {
    "52430b12-4d5f-d1e1-e063-6394a90abd64": {
      "match": "brand_token",
      "title": "SODIUM FLUORIDE RINSE LIQUID [ROCKLAND COSMETICS, INC.]",
      "spl_version": "1",
      "published_date": "2026-05-21"
    }
  },
  "productid": "0409-4888_9ee88abb-024a-4a3b-9776-1777eaf2f760",
  "productndc": "0409-4888",
  "dosage_form": "INJECTION, SOLUTION",
  "orange_book": {
    "appl_no": "018803",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AP",
        "strength": "90MG/10ML (9MG/ML)",
        "product_no": "001",
        "approval_date": "Oct 29, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AP",
        "strength": "180MG/20ML (9MG/ML)",
        "product_no": "002",
        "approval_date": "Oct 29, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AP",
        "strength": "450MG/50ML (9MG/ML)",
        "product_no": "003",
        "approval_date": "Oct 29, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "18MG/2ML (9MG/ML)",
        "product_no": "004",
        "approval_date": "Jan 22, 2015"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "27MG/3ML (9MG/ML)",
        "product_no": "005",
        "approval_date": "Jan 22, 2015"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "45MG/5ML (9MG/ML)",
        "product_no": "006",
        "approval_date": "Jan 22, 2015"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SODIUM CHLORIDE",
  "shortage_reason": "Sodium Oxybate Solution",
  "shortage_status": "current",
  "proprietary_name": "Sodium Chloride",
  "active_ingred_unit": "mg/mL",
  "application_number": "NDA018803",
  "marketing_category": "NDA",
  "nonproprietary_name": "Sodium Chloride",
  "start_marketing_date": "20050228",
  "active_numerator_strength": "9"
}

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