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United States · US · US:76420-325_34232f88-5219-6451-e063-6294a90a4469

MELOXICAM

Orange BookUNIISPLATC M01AC56

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

Identification

ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeM01AC56
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    7642032500
    1000 TABLET in 1 BOTTLE (76420-325-00)
  • ndc11
    7642032501
    100 TABLET in 1 BOTTLE (76420-325-01)
  • ndc11
    7642032505
    500 TABLET in 1 BOTTLE (76420-325-05)
  • ndc11
    7642032520
    20 TABLET in 1 BOTTLE (76420-325-20)
  • ndc11
    7642032530
    30 TABLET in 1 BOTTLE (76420-325-30)
  • ndc11
    7642032560
    60 TABLET in 1 BOTTLE (76420-325-60)
  • ndc11
    7642032590
    90 TABLET in 1 BOTTLE (76420-325-90)

Annotations

UNII (FDA Substance ID)
VG2QF83CGL
MELOXICAM
RxCUI 41493
Orange Book
A077929
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": "76420-325_34232f88-5219-6451-e063-6294a90a4469",
  "productndc": "76420-325",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077929",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "7.5MG",
        "product_no": "001",
        "approval_date": "Jul 19, 2006"
      },
      {
        "rs": false,
        "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": "ANDA077929",
  "marketing_category": "ANDA",
  "nonproprietary_name": "meloxicam",
  "start_marketing_date": "20060719",
  "active_numerator_strength": "7.5"
}

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