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United States · US · US:68071-3441_2d80b340-7ddc-adf0-e063-6294a90af485
Cefpodoxime Proxetil
Orange BookUNIISPLATC J01DD
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeJ01DD
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11680713441220 TABLET, FILM COATED in 1 BOTTLE (68071-3441-2)
Annotations
UNII (FDA Substance ID)
2TB00A1Z7N
CEFPODOXIME PROXETIL
RxCUI 47835
Orange Book
A210568
ABAB
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": "68071-3441_2d80b340-7ddc-adf0-e063-6294a90af485",
"productndc": "68071-3441",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "210568",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 100MG BASE",
"product_no": "001",
"approval_date": "May 18, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 200MG BASE",
"product_no": "002",
"approval_date": "May 18, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEFPODOXIME PROXETIL",
"proprietary_name": "Cefpodoxime Proxetil",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210568",
"marketing_category": "ANDA",
"nonproprietary_name": "Cefpodoxime Proxetil",
"start_marketing_date": "20230213",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code J01DD.
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