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United States · US · US:0574-0621_d2e70c5e-d4a9-4295-9eff-517ffb974e61
Podofilox
In shortageOrange BookUNIISPLATC D06BB04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPadagis US LLC
CountryUS (United States)
ATC codeD06BB04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1105740621053.5 g in 1 TUBE, WITH APPLICATOR (0574-0621-05)
Annotations
UNII (FDA Substance ID)
L36H50F353
PODOFILOX
RxCUI 8463
Orange Book
A211871
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Podofilox Topical Gel
Raw payload (JSON)
{
"unii": {
"unii": "L36H50F353",
"rxcui": "8463",
"inchikey": "YJGVMLPVUAXIQN-XVVDYKMHSA-N",
"display_name": "PODOFILOX",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"6af07697-5203-43e0-ba35-83683af851c3": {
"match": "brand_token",
"title": "PODOFILOX SOLUTION [PADAGIS US LLC]",
"spl_version": "9",
"published_date": "2024-03-12"
}
},
"productid": "0574-0621_d2e70c5e-d4a9-4295-9eff-517ffb974e61",
"productndc": "0574-0621",
"dosage_form": "GEL",
"orange_book": {
"appl_no": "211871",
"products": [
{
"rs": true,
"rld": false,
"te_code": null,
"strength": "0.5%",
"product_no": "001",
"approval_date": "Nov 22, 2023"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PODOFILOX",
"shortage_reason": "Podofilox Topical Gel",
"shortage_status": "current",
"proprietary_name": "Podofilox",
"active_ingred_unit": "mg/g",
"application_number": "ANDA211871",
"marketing_category": "ANDA",
"nonproprietary_name": "Podofilox",
"start_marketing_date": "20231213",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code D06BB04.
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