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United States · US · US:64850-440_97b69c02-a69e-46fe-8686-4b4d8ceb5dca
PHENDIMETRAZINE TARTRATE
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerElite Laboratories, Inc
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116485044001100 TABLET in 1 BOTTLE (64850-440-01)
- ndc1164850440101000 TABLET in 1 BOTTLE (64850-440-10)
Annotations
UNII (FDA Substance ID)
6985IP0T80
PHENDIMETRAZINE TARTRATE
RxCUI 58157
Orange Book
A040762
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "6985IP0T80",
"rxcui": "58157",
"inchikey": "VEPOHXYIFQMVHW-PVJVQHJQSA-N",
"display_name": "PHENDIMETRAZINE TARTRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"f5c30a88-5814-5b42-e053-2995a90a437a": {
"match": "brand_token",
"title": "PHENDIMETRAZINE TARTRATE TABLET [CALVIN SCOTT & CO., INC.]",
"spl_version": "3",
"published_date": "2026-06-01"
}
},
"productid": "64850-440_97b69c02-a69e-46fe-8686-4b4d8ceb5dca",
"productndc": "64850-440",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "040762",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AA",
"strength": "35MG",
"product_no": "001",
"approval_date": "Jan 28, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": "CIII",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PHENDIMETRAZINE TARTRATE",
"proprietary_name": "PHENDIMETRAZINE TARTRATE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA040762",
"marketing_category": "ANDA",
"nonproprietary_name": "Phendimetrazine Tartrate",
"start_marketing_date": "20121120",
"active_numerator_strength": "35"
}Access this data programmatically
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