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United States · US · US:50090-3226_3c117298-9cc5-4ebd-a581-82168ca396ae
Cefprozil
Orange BookUNIISPLATC J01DC
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeJ01DC
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11500903226050 mL in 1 BOTTLE (50090-3226-0)
Annotations
UNII (FDA Substance ID)
4W0459ZA4V
CEFPROZIL
RxCUI 19552
Orange Book
A065381
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4W0459ZA4V",
"rxcui": "19552",
"inchikey": null,
"display_name": "CEFPROZIL",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"800a2ec0-4798-4423-9613-d03024cf1f0e": {
"match": "brand_token",
"title": "CEFPROZIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.]",
"spl_version": "1",
"published_date": "2026-05-06"
}
},
"productid": "50090-3226_3c117298-9cc5-4ebd-a581-82168ca396ae",
"productndc": "50090-3226",
"dosage_form": "POWDER, FOR SUSPENSION",
"orange_book": {
"appl_no": "065381",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "125MG/5ML",
"product_no": "001",
"approval_date": "Jan 30, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "250MG/5ML",
"product_no": "002",
"approval_date": "Jan 30, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEFPROZIL",
"proprietary_name": "Cefprozil",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA065381",
"marketing_category": "ANDA",
"nonproprietary_name": "Cefprozil",
"start_marketing_date": "20070130",
"active_numerator_strength": "250"
}Related drugs
Other records sharing ATC code J01DC.
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