🇺🇸
United States · US · US:73473-902_98b3a053-2708-460d-9929-d89164cd4a49
DICYCLOMINE HYDROCHLORIDE
Orange BookUNIISPLATC A03AA07
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSolaris Pharma Corporation
CountryUS (United States)
ATC codeA03AA07
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc117347390201100 TABLET in 1 BOTTLE (73473-902-01)
- ndc1173473902101000 TABLET in 1 BOTTLE (73473-902-10)
Annotations
UNII (FDA Substance ID)
CQ903KQA31
DICYCLOMINE HYDROCHLORIDE
RxCUI 152021
Orange Book
A216760
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "CQ903KQA31",
"rxcui": "152021",
"inchikey": "GUBNMFJOJGDCEL-UHFFFAOYSA-N",
"display_name": "DICYCLOMINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"bb099db9-f635-4a64-8892-6236971dec45": {
"match": "brand_token",
"title": "DICYCLOMINE HYDROCHLORIDE SOLUTION [PAR HEALTH USA, LLC]",
"spl_version": "8",
"published_date": "2026-05-21"
}
},
"productid": "73473-902_98b3a053-2708-460d-9929-d89164cd4a49",
"productndc": "73473-902",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "216760",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "001",
"approval_date": "Nov 28, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DICYCLOMINE HYDROCHLORIDE",
"proprietary_name": "DICYCLOMINE HYDROCHLORIDE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA216760",
"marketing_category": "ANDA",
"nonproprietary_name": "DICYCLOMINE HYDROCHLORIDE",
"start_marketing_date": "20250610",
"active_numerator_strength": "20"
}Related drugs
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