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United States · US · US:71335-0406_e3af99c9-7276-462c-b374-1d71238c0693

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
    7133504060
    120 TABLET in 1 BOTTLE (71335-0406-0)
  • ndc11
    7133504061
    30 TABLET in 1 BOTTLE (71335-0406-1)
  • ndc11
    7133504062
    60 TABLET in 1 BOTTLE (71335-0406-2)
  • ndc11
    7133504063
    100 TABLET in 1 BOTTLE (71335-0406-3)
  • ndc11
    7133504064
    90 TABLET in 1 BOTTLE (71335-0406-4)
  • ndc11
    7133504065
    14 TABLET in 1 BOTTLE (71335-0406-5)
  • ndc11
    7133504066
    10 TABLET in 1 BOTTLE (71335-0406-6)
  • ndc11
    7133504067
    56 TABLET in 1 BOTTLE (71335-0406-7)
  • ndc11
    7133504068
    28 TABLET in 1 BOTTLE (71335-0406-8)
  • ndc11
    7133504069
    20 TABLET in 1 BOTTLE (71335-0406-9)

Annotations

UNII (FDA Substance ID)
VG2QF83CGL
MELOXICAM
RxCUI 41493
Orange Book
A077927
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": "71335-0406_e3af99c9-7276-462c-b374-1d71238c0693",
  "productndc": "71335-0406",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077927",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "7.5MG",
        "product_no": "001",
        "approval_date": "Dec 20, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "002",
        "approval_date": "Dec 20, 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": "ANDA077927",
  "marketing_category": "ANDA",
  "nonproprietary_name": "meloxicam",
  "start_marketing_date": "20070307",
  "active_numerator_strength": "7.5"
}

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