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United States · US · US:17856-5309_34f37e2c-ba78-120a-e063-6294a90aa750
Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerATLANTIC BIOLOGICALS CORP.
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc1117856530915 mL in 1 SYRINGE (17856-5309-1)
- ndc11178565309210 mL in 1 SYRINGE (17856-5309-2)
- ndc11178565309420 mL in 1 CUP (17856-5309-4)
- ndc1117856530955 mL in 1 CUP (17856-5309-5)
- ndc11178565309615 mL in 1 CUP (17856-5309-6)
- ndc1117856530977.5 mL in 1 CUP, UNIT-DOSE (17856-5309-7)
- ndc11178565309872 CUP, UNIT-DOSE in 1 CASE (17856-5309-8) / 10 mL in 1 CUP, UNIT-DOSE
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A074937
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": "17856-5309_34f37e2c-ba78-120a-e063-6294a90aa750",
"productndc": "17856-5309",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "074937",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "100MG/5ML",
"product_no": "001",
"approval_date": "Dec 22, 1998"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Ibuprofen",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA074937",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "19990207",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code G02CC01.
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