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United States · US · US:0023-6118_9f2892be-8330-4fd1-930e-b4d204df4e03
Condylox
In shortageOrange BookUNIISPLATC D06BB04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllergan, Inc.
CountryUS (United States)
ATC codeD06BB04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 0
No packs registered.
Annotations
UNII (FDA Substance ID)
L36H50F353
PODOFILOX
RxCUI 8463
Orange Book
N020529
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": {
"032e4bcb-b1ed-4029-b2a6-e92f3bf5cc37": {
"match": "brand_token",
"title": "CONDYLOX (PODOFILOX) GEL [ALLERGAN, INC.]",
"spl_version": "8",
"published_date": "2025-12-05"
}
},
"productid": "0023-6118_9f2892be-8330-4fd1-930e-b4d204df4e03",
"productndc": "0023-6118",
"dosage_form": "GEL",
"orange_book": {
"appl_no": "020529",
"products": [
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "0.5%",
"product_no": "001",
"approval_date": "Mar 13, 1997"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PODOFILOX",
"shortage_reason": "Podofilox Topical Gel",
"shortage_status": "current",
"proprietary_name": "Condylox",
"active_ingred_unit": "mg/g",
"application_number": "NDA020529",
"marketing_category": "NDA",
"nonproprietary_name": "podofilox",
"start_marketing_date": "19970313",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code D06BB04.
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