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United States · US · US:64980-402_803b37ff-46c6-4dcb-9d9f-a118c4c4601b
Cefpodoxime Proxetil
Orange BookUNIISPLATC J01DD
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRising Pharma Holdings, Inc.
CountryUS (United States)
ATC codeJ01DD
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1164980402101 BOTTLE in 1 CARTON (64980-402-10) / 100 mL in 1 BOTTLE
- ndc1164980402501 BOTTLE in 1 CARTON (64980-402-50) / 50 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
2TB00A1Z7N
CEFPODOXIME PROXETIL
RxCUI 47835
Orange Book
A065409
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "2TB00A1Z7N",
"rxcui": "47835",
"inchikey": "LTINZAODLRIQIX-FBXRGJNPSA-N",
"display_name": "CEFPODOXIME PROXETIL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"ca125f98-0ea7-43c3-9861-9dada1efef45": {
"match": "brand_token",
"title": "CEFPODOXIME PROXETIL POWDER [AX PHARMACEUTICAL CORP]",
"spl_version": "5",
"published_date": "2026-05-11"
}
},
"productid": "64980-402_803b37ff-46c6-4dcb-9d9f-a118c4c4601b",
"productndc": "64980-402",
"dosage_form": "GRANULE, FOR SUSPENSION",
"orange_book": {
"appl_no": "065409",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 50MG BASE/5ML",
"product_no": "001",
"approval_date": "Jun 8, 2007"
},
{
"rs": true,
"rld": false,
"te_code": null,
"strength": "EQ 100MG BASE/5ML",
"product_no": "002",
"approval_date": "Jun 8, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEFPODOXIME PROXETIL",
"proprietary_name": "Cefpodoxime Proxetil",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA065409",
"marketing_category": "ANDA",
"nonproprietary_name": "Cefpodoxime Proxetil",
"start_marketing_date": "20070608",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code J01DD.
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