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United States · US · US:76420-039_2d871eb9-b21b-4113-e063-6294a90a118c

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 · 11

  • ndc11
    7642003900
    1000 TABLET in 1 BOTTLE (76420-039-00)
  • ndc11
    7642003901
    100 TABLET in 1 BOTTLE (76420-039-01)
  • ndc11
    7642003905
    500 TABLET in 1 BOTTLE (76420-039-05)
  • ndc11
    7642003907
    7 TABLET in 1 BOTTLE (76420-039-07)
  • ndc11
    7642003910
    10 TABLET in 1 BOTTLE (76420-039-10)
  • ndc11
    7642003914
    14 TABLET in 1 BOTTLE (76420-039-14)
  • ndc11
    7642003920
    20 TABLET in 1 BOTTLE (76420-039-20)
  • ndc11
    7642003930
    30 TABLET in 1 BOTTLE (76420-039-30)
  • ndc11
    7642003955
    5000 TABLET in 1 BOTTLE (76420-039-55)
  • ndc11
    7642003960
    60 TABLET in 1 BOTTLE (76420-039-60)
  • ndc11
    7642003990
    90 TABLET in 1 BOTTLE (76420-039-90)

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": "76420-039_2d871eb9-b21b-4113-e063-6294a90a118c",
  "productndc": "76420-039",
  "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": "15"
}

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