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United States · US · US:10702-044_1764f49c-0f71-0bfc-e063-6294a90a8a48
DIETHYLPROPION HYDROCHLORIDE
Orange BookUNIISPLATC A08AA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKVK-TECH, INC
CountryUS (United States)
ATC codeA08AA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc111070204401100 TABLET in 1 BOTTLE (10702-044-01)
- ndc11107020440330 TABLET in 1 BOTTLE (10702-044-03)
- ndc11107020440660 TABLET in 1 BOTTLE (10702-044-06)
Annotations
UNII (FDA Substance ID)
19V2PL39NG
DIETHYLPROPION HYDROCHLORIDE
RxCUI 81998
Orange Book
A201212
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "19V2PL39NG",
"rxcui": "81998",
"inchikey": "ICFXZZFWRWNZMA-UHFFFAOYSA-N",
"display_name": "DIETHYLPROPION HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"04f1a804-00f1-48f5-acfa-0ed1a8544784": {
"match": "brand_token",
"title": "DIETHYLPROPION HYDROCHLORIDE ER (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS]",
"spl_version": "29",
"published_date": "2026-06-01"
}
},
"productid": "10702-044_1764f49c-0f71-0bfc-e063-6294a90a8a48",
"productndc": "10702-044",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "201212",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AA",
"strength": "25MG",
"product_no": "001",
"approval_date": "Dec 22, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": "CIV",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIETHYLPROPION HYDROCHLORIDE",
"proprietary_name": "DIETHYLPROPION HYDROCHLORIDE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA201212",
"marketing_category": "ANDA",
"nonproprietary_name": "DIETHYLPROPION HYDROCHLORIDE",
"start_marketing_date": "20101227",
"active_numerator_strength": "25"
}Related drugs
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