🇺🇸
United States · US · US:72789-256_2e5c9777-8e42-bc90-e063-6294a90a1ee8
Clorazepate Dipotassium
Orange BookUNIISPLATC N05BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeN05BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1172789256066 TABLET in 1 BOTTLE, PLASTIC (72789-256-06)
Annotations
UNII (FDA Substance ID)
63FN7G03XY
CLORAZEPATE DIPOTASSIUM
RxCUI 2607
Orange Book
A075731
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "63FN7G03XY",
"rxcui": "2607",
"inchikey": "QCHSEDTUUKDTIG-UHFFFAOYSA-L",
"display_name": "CLORAZEPATE DIPOTASSIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"919cbd07-f587-4005-acff-26213dd1d1fb": {
"match": "brand_token",
"title": "CLORAZEPATE DIPOTASSIUM TABLET [AUROLIFE PHARMA LLC]",
"spl_version": "5",
"published_date": "2026-03-26"
}
},
"productid": "72789-256_2e5c9777-8e42-bc90-e063-6294a90a1ee8",
"productndc": "72789-256",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "075731",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "15MG",
"product_no": "001",
"approval_date": "Apr 27, 2000"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "7.5MG",
"product_no": "002",
"approval_date": "Apr 27, 2000"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "3.75MG",
"product_no": "003",
"approval_date": "Apr 27, 2000"
}
],
"appl_type": "A"
},
"dea_schedule": "CIV",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CLORAZEPATE DIPOTASSIUM",
"proprietary_name": "Clorazepate Dipotassium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075731",
"marketing_category": "ANDA",
"nonproprietary_name": "Clorazepate Dipotassium",
"start_marketing_date": "20000427",
"active_numerator_strength": "15"
}Related drugs
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