🇺🇸
United States · US · US:30142-050_2a2bd653-3e02-4f81-bd07-0c3506215ea3
ibuprofen pm
Orange BookUNIISPLATC D04AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKroger Company
CountryUS (United States)
ATC codeD04AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1130142050271 BOTTLE in 1 CARTON (30142-050-27) / 80 TABLET, FILM COATED in 1 BOTTLE
- ndc1130142050601 BOTTLE in 1 CARTON (30142-050-60) / 20 TABLET, FILM COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
4OD433S209
DIPHENHYDRAMINE CITRATE
RxCUI 82004
Orange Book
A079113
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4OD433S209",
"rxcui": "82004",
"inchikey": "SPCKHVPPRJWQRZ-UHFFFAOYSA-N",
"display_name": "DIPHENHYDRAMINE CITRATE",
"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": "30142-050_2a2bd653-3e02-4f81-bd07-0c3506215ea3",
"productndc": "30142-050",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "079113",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "38MG;200MG",
"product_no": "001",
"approval_date": "Dec 22, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE CITRATE; IBUPROFEN",
"proprietary_name": "ibuprofen pm",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA079113",
"marketing_category": "ANDA",
"nonproprietary_name": "diphenhydramine citrate, ibuprofen",
"start_marketing_date": "20090406",
"active_numerator_strength": "38; 200"
}Related drugs
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