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United States · US · US:71335-2717_cf7644ae-e852-48ba-a72a-f53743ddd5cb
Ciclopirox Olamine
Orange BookUNIISPLATC D01AE
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeD01AE
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1171335271711 BOTTLE in 1 CARTON (71335-2717-1) / 60 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
50MD4SB4AP
CICLOPIROX OLAMINE
RxCUI 52172
Orange Book
A077676
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "50MD4SB4AP",
"rxcui": "52172",
"inchikey": "MBRHNTMUYWQHMR-UHFFFAOYSA-N",
"display_name": "CICLOPIROX OLAMINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"1a74ed86-997a-4b86-b54a-b2b2c94e8abb": {
"match": "brand_token",
"title": "CICLOPIROX OLAMINE CREAM [PADAGIS ISRAEL PHARMACEUTICALS LTD]",
"spl_version": "14",
"published_date": "2026-04-17"
}
},
"productid": "71335-2717_cf7644ae-e852-48ba-a72a-f53743ddd5cb",
"productndc": "71335-2717",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "077676",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "0.77%",
"product_no": "001",
"approval_date": "Dec 15, 2006"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CICLOPIROX OLAMINE",
"proprietary_name": "Ciclopirox Olamine",
"active_ingred_unit": "mg/100mL",
"application_number": "ANDA077676",
"marketing_category": "ANDA",
"nonproprietary_name": "Ciclopirox Olamine",
"start_marketing_date": "20061229",
"active_numerator_strength": "7.7"
}Related drugs
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