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United States · US · US:71335-1956_e762265a-1e60-4f9c-95dc-173aa8fb8eed

meloxicam

Orange BookUNIISPLATC M01AC56

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeM01AC56
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133519560
    20 TABLET in 1 BOTTLE (71335-1956-0)
  • ndc11
    7133519561
    30 TABLET in 1 BOTTLE (71335-1956-1)
  • ndc11
    7133519562
    60 TABLET in 1 BOTTLE (71335-1956-2)
  • ndc11
    7133519563
    90 TABLET in 1 BOTTLE (71335-1956-3)
  • ndc11
    7133519564
    14 TABLET in 1 BOTTLE (71335-1956-4)
  • ndc11
    7133519565
    100 TABLET in 1 BOTTLE (71335-1956-5)
  • ndc11
    7133519566
    7 TABLET in 1 BOTTLE (71335-1956-6)
  • ndc11
    7133519567
    10 TABLET in 1 BOTTLE (71335-1956-7)
  • ndc11
    7133519568
    15 TABLET in 1 BOTTLE (71335-1956-8)
  • ndc11
    7133519569
    28 TABLET in 1 BOTTLE (71335-1956-9)

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": "71335-1956_e762265a-1e60-4f9c-95dc-173aa8fb8eed",
  "productndc": "71335-1956",
  "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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