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United States · US · US:71205-924_24995687-1075-4f4b-a198-460fd1f8b7d9

Meloxicam

Orange BookUNIISPLATC M01AC56

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

Identification

ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeM01AC56
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 11

  • ndc11
    7120592400
    100 TABLET in 1 BOTTLE, PLASTIC (71205-924-00)
  • ndc11
    7120592407
    7 TABLET in 1 BOTTLE, PLASTIC (71205-924-07)
  • ndc11
    7120592411
    1000 TABLET in 1 BOTTLE, PLASTIC (71205-924-11)
  • ndc11
    7120592414
    14 TABLET in 1 BOTTLE, PLASTIC (71205-924-14)
  • ndc11
    7120592415
    15 TABLET in 1 BOTTLE, PLASTIC (71205-924-15)
  • ndc11
    7120592428
    28 TABLET in 1 BOTTLE, PLASTIC (71205-924-28)
  • ndc11
    7120592430
    30 TABLET in 1 BOTTLE, PLASTIC (71205-924-30)
  • ndc11
    7120592455
    500 TABLET in 1 BOTTLE, PLASTIC (71205-924-55)
  • ndc11
    7120592460
    60 TABLET in 1 BOTTLE, PLASTIC (71205-924-60)
  • ndc11
    7120592472
    120 TABLET in 1 BOTTLE, PLASTIC (71205-924-72)
  • ndc11
    7120592490
    90 TABLET in 1 BOTTLE, PLASTIC (71205-924-90)

Annotations

UNII (FDA Substance ID)
VG2QF83CGL
MELOXICAM
RxCUI 41493
Orange Book
A077918
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": "71205-924_24995687-1075-4f4b-a198-460fd1f8b7d9",
  "productndc": "71205-924",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077918",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "7.5MG",
        "product_no": "001",
        "approval_date": "Dec 7, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "15MG",
        "product_no": "002",
        "approval_date": "Dec 7, 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": "ANDA077918",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Meloxicam",
  "start_marketing_date": "20100630",
  "active_numerator_strength": "15"
}

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