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United States · US · US:0904-5307_4b4333df-2739-654b-e063-6394a90a4a1d
Banophen
UNIISPLATC D04AA32
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMajor Pharmaceuticals
CountryUS (United States)
ATC codeD04AA32
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc110904530760100 CAPSULE in 1 BOTTLE (0904-5307-60)
- ndc1109045307801000 CAPSULE in 1 BOTTLE (0904-5307-80)
Annotations
UNII (FDA Substance ID)
TC2D6JAD40
DIPHENHYDRAMINE HYDROCHLORIDE
RxCUI 1362
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "TC2D6JAD40",
"rxcui": "1362",
"inchikey": "PCHPORCSPXIHLZ-UHFFFAOYSA-N",
"display_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"20f00537-2c8a-45d1-8e5f-ec276d0a47b6": {
"match": "brand_token",
"title": "BANOPHEN (DIPHENHYDRAMINE HCL) CAPSULE [BRYANT RANCH PREPACK]",
"spl_version": "11",
"published_date": "2026-05-21"
}
},
"productid": "0904-5307_4b4333df-2739-654b-e063-6394a90a4a1d",
"productndc": "0904-5307",
"dosage_form": "CAPSULE",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"proprietary_name": "Banophen",
"active_ingred_unit": "mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "diphenhydramine hcl",
"start_marketing_date": "20091102",
"active_numerator_strength": "50"
}Related drugs
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