Meloxicam

Orange BookUNIISPLATC M01AC56

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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
7133518880
20 TABLET in 1 BOTTLE, PLASTIC (71335-1888-0)
ndc11
7133518881
30 TABLET in 1 BOTTLE, PLASTIC (71335-1888-1)
ndc11
7133518882
60 TABLET in 1 BOTTLE, PLASTIC (71335-1888-2)
ndc11
7133518883
90 TABLET in 1 BOTTLE, PLASTIC (71335-1888-3)
ndc11
7133518884
14 TABLET in 1 BOTTLE, PLASTIC (71335-1888-4)
ndc11
7133518885
100 TABLET in 1 BOTTLE, PLASTIC (71335-1888-5)
ndc11
7133518886
7 TABLET in 1 BOTTLE, PLASTIC (71335-1888-6)
ndc11
7133518887
10 TABLET in 1 BOTTLE, PLASTIC (71335-1888-7)
ndc11
7133518888
15 TABLET in 1 BOTTLE, PLASTIC (71335-1888-8)
ndc11
7133518889
28 TABLET in 1 BOTTLE, PLASTIC (71335-1888-9)

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": "71335-1888_dd196452-e484-4e92-901c-3dbb9c4c78e3",
  "productndc": "71335-1888",
  "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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