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United States · US · US:57344-090_284d200c-7ba4-d545-e063-6394a90a4d51
Diphenhydramine
UNIISPLATC D04AA32
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAAA Pharmaceutical, Inc.
CountryUS (United States)
ATC codeD04AA32
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1157344090024 BLISTER PACK in 1 CARTON (57344-090-02) / 12 TABLET, COATED in 1 BLISTER PACK
- ndc1157344090031 BOTTLE, PLASTIC in 1 CARTON (57344-090-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
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": {
"48ede5ab-207b-cf0c-e063-6394a90a419f": {
"match": "brand_token",
"title": "DIPHENHYDRAMINE ORAL SOLUTION (DIPHENHYDRAMINE HCL12.5MG/5ML) SOLUTION [ALDAMA PHARMACEUTICALS, INC]",
"spl_version": "3",
"published_date": "2026-06-02"
}
},
"productid": "57344-090_284d200c-7ba4-d545-e063-6394a90a4d51",
"productndc": "57344-090",
"dosage_form": "TABLET, COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"proprietary_name": "Diphenhydramine",
"active_ingred_unit": "mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"start_marketing_date": "20120413",
"active_numerator_strength": "25"
}Related drugs
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