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United States · US · US:83980-030_4064e892-4c7a-46a7-9114-3e2bf466e597
etodolac
Orange BookUNIISPLATC M01AB08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerIpca Laboratories Limited
CountryUS (United States)
ATC codeM01AB08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc118398003001100 TABLET in 1 BOTTLE (83980-030-01)
- ndc118398003005500 TABLET in 1 BOTTLE (83980-030-05)
- ndc11839800301330 TABLET in 1 BOTTLE (83980-030-13)
Annotations
UNII (FDA Substance ID)
2M36281008
ETODOLAC
RxCUI 24605
Orange Book
A204729
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2M36281008",
"rxcui": "24605",
"inchikey": "NNYBQONXHNTVIJ-UHFFFAOYSA-N",
"display_name": "ETODOLAC",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"007c55fa-ef8b-4a8e-bfe5-e47c6e5da727": {
"match": "brand_token",
"title": "ETODOLAC TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "26",
"published_date": "2026-05-25"
}
},
"productid": "83980-030_4064e892-4c7a-46a7-9114-3e2bf466e597",
"productndc": "83980-030",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "204729",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "May 1, 2024"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "002",
"approval_date": "May 1, 2024"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ETODOLAC",
"proprietary_name": "etodolac",
"active_ingred_unit": "mg/1",
"application_number": "ANDA204729",
"marketing_category": "ANDA",
"nonproprietary_name": "etodolac",
"start_marketing_date": "20260213",
"active_numerator_strength": "500"
}Related drugs
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