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United States · US · US:50090-5339_860ed0f5-9a2b-4c14-b7e6-b2d5336078b2

meloxicam

Orange BookUNIISPLATC M01AC56

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

Identification

ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeM01AC56
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    5009053390
    7 TABLET in 1 BOTTLE (50090-5339-0)
  • ndc11
    5009053391
    14 TABLET in 1 BOTTLE (50090-5339-1)
  • ndc11
    5009053392
    30 TABLET in 1 BOTTLE (50090-5339-2)
  • ndc11
    5009053393
    60 TABLET in 1 BOTTLE (50090-5339-3)
  • ndc11
    5009053394
    100 TABLET in 1 BOTTLE (50090-5339-4)
  • ndc11
    5009053396
    90 TABLET in 1 BOTTLE (50090-5339-6)
  • ndc11
    5009053397
    10 TABLET in 1 BOTTLE (50090-5339-7)

Annotations

UNII (FDA Substance ID)
VG2QF83CGL
MELOXICAM
RxCUI 41493
Orange Book
A077921
ABAB
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": "50090-5339_860ed0f5-9a2b-4c14-b7e6-b2d5336078b2",
  "productndc": "50090-5339",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077921",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "7.5MG",
        "product_no": "001",
        "approval_date": "Jul 19, 2006"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "002",
        "approval_date": "Jul 19, 2006"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MELOXICAM",
  "proprietary_name": "meloxicam",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077921",
  "marketing_category": "ANDA",
  "nonproprietary_name": "meloxicam",
  "start_marketing_date": "20060719",
  "active_numerator_strength": "15"
}

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