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United States · US · US:70518-0200_4af35f0c-4bd3-961e-e063-6294a90ad786
MELOXICAM
Orange BookUNIISPLATC M01AC56
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerREMEDYREPACK INC.
CountryUS (United States)
ATC codeM01AC56
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11705180200030 TABLET in 1 BLISTER PACK (70518-0200-0)
- ndc11705180200130 TABLET in 1 BOTTLE, PLASTIC (70518-0200-1)
- ndc11705180200390 TABLET in 1 BOTTLE, PLASTIC (70518-0200-3)
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": "70518-0200_4af35f0c-4bd3-961e-e063-6294a90ad786",
"productndc": "70518-0200",
"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": "20170206",
"active_numerator_strength": "15"
}Related drugs
Other records sharing ATC code M01AC56.
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