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United States · US · US:59556-895_7d889b12-7d30-423f-a988-bb1d201ebb59
IBUPROFEN
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerStrides Pharma Inc
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc1159556895131 BOTTLE in 1 CARTON (59556-895-13) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1159556895291 BOTTLE in 1 CARTON (59556-895-29) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1159556895391 BOTTLE in 1 CARTON (59556-895-39) / 200 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1159556895481 BOTTLE in 1 CARTON (59556-895-48) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1159556895501 BOTTLE in 1 CARTON (59556-895-50) / 300 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1159556895797000 CAPSULE, LIQUID FILLED in 1 BAG (59556-895-79)
- ndc1159556895851 BOTTLE in 1 CARTON (59556-895-85) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1159556895861 BOTTLE in 1 CARTON (59556-895-86) / 120 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1159556895871 BOTTLE in 1 CARTON (59556-895-87) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE
- ndc1159556895881 BOTTLE in 1 CARTON (59556-895-88) / 300 CAPSULE, LIQUID FILLED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A204469
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WK2XYI10QM",
"rxcui": "5640",
"inchikey": "HEFNNWSXXWATRW-UHFFFAOYSA-N",
"display_name": "IBUPROFEN",
"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": "59556-895_7d889b12-7d30-423f-a988-bb1d201ebb59",
"productndc": "59556-895",
"dosage_form": "CAPSULE, LIQUID FILLED",
"orange_book": {
"appl_no": "204469",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 200MG FREE ACID AND POTASSIUM SALT",
"product_no": "001",
"approval_date": "Mar 28, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "IBUPROFEN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA204469",
"marketing_category": "ANDA",
"nonproprietary_name": "IBUPROFEN",
"start_marketing_date": "20221116",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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