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United States · US · US:0276-0506_4add4a71-ad1b-2577-e063-6294a90a3263
Ketoprofen
Orange BookUNIISPLATC M01AE53
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMisemer Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeM01AE53
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110276050610100 CAPSULE in 1 BOTTLE (0276-0506-10)
Annotations
UNII (FDA Substance ID)
90Y4QC304K
KETOPROFEN
RxCUI 6142
Orange Book
A074014
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "90Y4QC304K",
"rxcui": "6142",
"inchikey": "DKYWVDODHFEZIM-UHFFFAOYSA-N",
"display_name": "KETOPROFEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"4e7bceb6-dcb5-c5e0-e063-6294a90a101e": {
"match": "brand_token",
"title": "KETOPROFEN CAPSULE [MARNEL PHARMACEUTICALS, INC.]",
"spl_version": "1",
"published_date": "2026-04-14"
}
},
"productid": "0276-0506_4add4a71-ad1b-2577-e063-6294a90a3263",
"productndc": "0276-0506",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "074014",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "25MG",
"product_no": "001",
"approval_date": "Jan 29, 1993"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Jan 29, 1993"
},
{
"rs": true,
"rld": false,
"te_code": null,
"strength": "75MG",
"product_no": "003",
"approval_date": "Jan 29, 1993"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "KETOPROFEN",
"proprietary_name": "Ketoprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074014",
"marketing_category": "ANDA",
"nonproprietary_name": "Ketoprofen",
"start_marketing_date": "20220913",
"active_numerator_strength": "50"
}Related drugs
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