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United States · US · US:59212-601_5b7465cd-3367-44ee-a11d-d021d6400a23
PANRETIN
Orange BookUNIISPLATC D11AH04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAdvanz Pharma (US) Corp.
CountryUS (United States)
ATC codeD11AH04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11592126012260 g in 1 TUBE (59212-601-22)
Annotations
UNII (FDA Substance ID)
1UA8E65KDZ
ALITRETINOIN
RxCUI 81864
Orange Book
N020886
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "1UA8E65KDZ",
"rxcui": "81864",
"inchikey": "SHGAZHPCJJPHSC-ZVCIMWCZSA-N",
"display_name": "ALITRETINOIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"49c16717-7d86-4257-80c9-baa1417e5555": {
"match": "brand_token",
"title": "PANRETIN (ALITRETINOIN) GEL [ADVANZ PHARMA (US) CORP.]",
"spl_version": "6",
"published_date": "2025-12-04"
}
},
"productid": "59212-601_5b7465cd-3367-44ee-a11d-d021d6400a23",
"productndc": "59212-601",
"dosage_form": "GEL",
"orange_book": {
"appl_no": "020886",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 0.1% BASE",
"product_no": "001",
"approval_date": "Feb 2, 1999"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ALITRETINOIN",
"proprietary_name": "PANRETIN",
"active_ingred_unit": "mg/60g",
"application_number": "NDA020886",
"marketing_category": "NDA",
"nonproprietary_name": "alitretinoin",
"start_marketing_date": "20190910",
"active_numerator_strength": "60"
}Related drugs
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