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United States · US · US:63029-554_322a3f7f-6a0f-43b9-9819-9ec52e856404
Sominex
UNIISPLATC D04AA32
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMedtech Products Inc.
CountryUS (United States)
ATC codeD04AA32
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1163029554019 BLISTER PACK in 1 BOX (63029-554-01) / 8 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1163029554162 BLISTER PACK in 1 BOX (63029-554-16) / 8 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1163029554324 BLISTER PACK in 1 BOX (63029-554-32) / 8 TABLET, FILM COATED in 1 BLISTER PACK
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": {
"f7858ecf-8498-4465-85d8-3e7814737573": {
"match": "brand_token",
"title": "SOMINEX (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [MEDTECH PRODUCTS INC.]",
"spl_version": "3",
"published_date": "2025-11-17"
}
},
"productid": "63029-554_322a3f7f-6a0f-43b9-9819-9ec52e856404",
"productndc": "63029-554",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"proprietary_name": "Sominex",
"active_ingred_unit": "mg/1",
"application_number": "M010",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
"start_marketing_date": "20120601",
"active_numerator_strength": "25"
}Related drugs
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