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United States · US · US:42806-566_d7a3306e-01d4-4966-a473-62136d81f959
CHLORDIAZEPOXIDE HYDROCHLORIDE
Orange BookUNIISPLATC N05BA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEpic Pharma, LLC
CountryUS (United States)
ATC codeN05BA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc114280656601100 CAPSULE, GELATIN COATED in 1 BOTTLE (42806-566-01)
Annotations
UNII (FDA Substance ID)
MFM6K1XWDK
CHLORDIAZEPOXIDE HYDROCHLORIDE
RxCUI 203173
Orange Book
A085475
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "MFM6K1XWDK",
"rxcui": "203173",
"inchikey": "DMLFJMQTNDSRFU-UHFFFAOYSA-N",
"display_name": "CHLORDIAZEPOXIDE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"511264f5-024b-350a-e063-6394a90a51e9": {
"match": "brand_token",
"title": "CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE [COUPER LLC]",
"spl_version": "1",
"published_date": "2026-05-07"
}
},
"productid": "42806-566_d7a3306e-01d4-4966-a473-62136d81f959",
"productndc": "42806-566",
"dosage_form": "CAPSULE, GELATIN COATED",
"orange_book": {
"appl_no": "085475",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "A"
},
"dea_schedule": "CIV",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CHLORDIAZEPOXIDE HYDROCHLORIDE",
"proprietary_name": "CHLORDIAZEPOXIDE HYDROCHLORIDE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA085475",
"marketing_category": "ANDA",
"nonproprietary_name": "CHLORDIAZEPOXIDE HYDROCHLORIDE",
"start_marketing_date": "20210813",
"active_numerator_strength": "25"
}Related drugs
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