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United States · US · US:24208-735_34fff06e-fa45-478a-b136-e019483fa07d
Cyclopentolate Hydrochloride
Orange BookUNIIATC S01FA54
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBausch & Lomb Incorporated
CountryUS (United States)
ATC codeS01FA54
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1124208735011 BOTTLE, DROPPER in 1 CARTON (24208-735-01) / 2 mL in 1 BOTTLE, DROPPER
- ndc1124208735061 BOTTLE, DROPPER in 1 CARTON (24208-735-06) / 15 mL in 1 BOTTLE, DROPPER
Annotations
UNII (FDA Substance ID)
736I6971TE
CYCLOPENTOLATE HYDROCHLORIDE
RxCUI 106029
Orange Book
A040075
AT
Raw payload (JSON)
{
"unii": {
"unii": "736I6971TE",
"rxcui": "106029",
"inchikey": "RHKZVMUBMXGOLL-UHFFFAOYSA-N",
"display_name": "CYCLOPENTOLATE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "OPHTHALMIC",
"productid": "24208-735_34fff06e-fa45-478a-b136-e019483fa07d",
"productndc": "24208-735",
"dosage_form": "SOLUTION/ DROPS",
"orange_book": {
"appl_no": "040075",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AT",
"strength": "1%",
"product_no": "001",
"approval_date": "Apr 29, 1994"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CYCLOPENTOLATE HYDROCHLORIDE",
"proprietary_name": "Cyclopentolate Hydrochloride",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA040075",
"marketing_category": "ANDA",
"nonproprietary_name": "Cyclopentolate Hydrochloride",
"start_marketing_date": "19940429",
"active_numerator_strength": "10"
}Related drugs
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- GBMydrilate 0.5% solutionEsteve Pharmaceuticals Ltd
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