🇺🇸
United States · US · US:59651-908_21688404-41fb-487e-8ba0-aea4431a42fa
Ibuprofen and famotidine
Orange BookUNIISPLATC A02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAurobindo Pharma Limited
CountryUS (United States)
ATC codeA02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11596519089090 TABLET, FILM COATED in 1 BOTTLE (59651-908-90)
Annotations
UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A219538
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5QZO15J2Z8",
"rxcui": "4278",
"inchikey": "XUFQPHANEAPEMJ-UHFFFAOYSA-N",
"display_name": "FAMOTIDINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"aeee629b-255c-40d8-8e95-779aec00f723": {
"match": "brand_token",
"title": "IBUPROFEN TABLET [NORTHSTAR RX LLC]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "59651-908_21688404-41fb-487e-8ba0-aea4431a42fa",
"productndc": "59651-908",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "219538",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "26.6MG;800MG",
"product_no": "001",
"approval_date": "Jun 30, 2025"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "FAMOTIDINE; IBUPROFEN",
"proprietary_name": "Ibuprofen and famotidine",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA219538",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen and famotidine",
"start_marketing_date": "20250630",
"active_numerator_strength": "26.6; 800"
}Related drugs
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