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United States · US · US:67296-1472_2c62c754-9698-47f7-e063-6294a90a94fe
anti diarrheal
Orange BookUNIISPLATC A07DA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRedpharm Drug Inc
CountryUS (United States)
ATC codeA07DA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11672961472724 TABLET, FILM COATED in 1 BOTTLE (67296-1472-7)
Annotations
UNII (FDA Substance ID)
77TI35393C
LOPERAMIDE HYDROCHLORIDE
RxCUI 82038
Orange Book
A075232
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "77TI35393C",
"rxcui": "82038",
"inchikey": "PGYPOBZJRVSMDS-UHFFFAOYSA-N",
"display_name": "LOPERAMIDE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"dd993f38-a31f-4739-9496-e14186a89053": {
"match": "brand_token",
"title": "ANTI DIARRHEAL (LOPERAMIDE HCL) TABLET [CHAIN DRUG MARKETING ASSOCIATION, INC.]",
"spl_version": "6",
"published_date": "2026-05-21"
}
},
"productid": "67296-1472_2c62c754-9698-47f7-e063-6294a90a94fe",
"productndc": "67296-1472",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "075232",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "2MG",
"product_no": "001",
"approval_date": "Jan 6, 2000"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LOPERAMIDE HYDROCHLORIDE",
"proprietary_name": "anti diarrheal",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075232",
"marketing_category": "ANDA",
"nonproprietary_name": "Loperamide Hydrochloride",
"start_marketing_date": "20030224",
"active_numerator_strength": "2"
}Related drugs
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