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United States · US · US:71205-611_449c7ca6-7fd4-4728-b330-2a3e261c6693
Banophen
UNIISPLATC D04AA32
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeD04AA32
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11712056112020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-20)
- ndc11712056113030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-30)
- ndc11712056116060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-60)
- ndc11712056119090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-90)
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": "71205-611_449c7ca6-7fd4-4728-b330-2a3e261c6693",
"productndc": "71205-611",
"dosage_form": "TABLET, FILM COATED",
"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": "19900302",
"active_numerator_strength": "25"
}Related drugs
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