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United States · US · US:72919-124_99836a73-8344-4ed4-a0d5-b813619da5b1

Meloxicam

Orange BookUNIISPLATC M01AC56

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

Identification

ManufacturerEmerald Therapeutics, LLC
CountryUS (United States)
ATC codeM01AC56
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7291912410
    1 BOTTLE, PLASTIC in 1 CARTON (72919-124-10) / 100 mL in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
VG2QF83CGL
MELOXICAM
RxCUI 41493
Orange Book
N021530
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "VG2QF83CGL",
    "rxcui": "41493",
    "inchikey": "ZRVUJXDFFKFLMG-UHFFFAOYSA-N",
    "display_name": "MELOXICAM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4ddf5a4d-8e84-419d-8e3a-c91b85501885": {
      "match": "brand_token",
      "title": "MELOXICAM SUSPENSION [AVONDALE PHARMACEUTICALS, LLC]",
      "spl_version": "3",
      "published_date": "2026-06-01"
    }
  },
  "productid": "72919-124_99836a73-8344-4ed4-a0d5-b813619da5b1",
  "productndc": "72919-124",
  "dosage_form": "SUSPENSION",
  "orange_book": {
    "appl_no": "021530",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "7.5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
        "product_no": "001",
        "approval_date": "Jun 1, 2004"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MELOXICAM",
  "proprietary_name": "Meloxicam",
  "active_ingred_unit": "mg/5mL",
  "application_number": "NDA021530",
  "marketing_category": "NDA AUTHORIZED GENERIC",
  "nonproprietary_name": "MELOXICAM",
  "start_marketing_date": "20051101",
  "active_numerator_strength": "7.5"
}

Related drugs

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