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United States · US · US:69584-181_6cf8d202-17fc-4c56-be33-4d74f6591077
Dipyridamole
Orange BookUNIISPLATC B01AC07
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerOxford Pharmaceuticals, LLC
CountryUS (United States)
ATC codeB01AC07
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116958418110100 TABLET, FILM COATED in 1 BOTTLE (69584-181-10)
Annotations
UNII (FDA Substance ID)
64ALC7F90C
DIPYRIDAMOLE
RxCUI 3521
Orange Book
A040542
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "64ALC7F90C",
"rxcui": "3521",
"inchikey": "IZEKFCXSFNUWAM-UHFFFAOYSA-N",
"display_name": "DIPYRIDAMOLE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"226099e2-70bb-4b9b-bb52-c20fbca2aec5": {
"match": "brand_token",
"title": "DIPYRIDAMOLE TABLET, FILM COATED [REMEDYREPACK INC.]",
"spl_version": "1",
"published_date": "2026-04-30"
}
},
"productid": "69584-181_6cf8d202-17fc-4c56-be33-4d74f6591077",
"productndc": "69584-181",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "040542",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Apr 21, 2006"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Apr 21, 2006"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "75MG",
"product_no": "003",
"approval_date": "Apr 21, 2006"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DIPYRIDAMOLE",
"proprietary_name": "Dipyridamole",
"active_ingred_unit": "mg/1",
"application_number": "ANDA040542",
"marketing_category": "ANDA",
"nonproprietary_name": "Dipyridamole",
"start_marketing_date": "20210415",
"active_numerator_strength": "25"
}Related drugs
Other records sharing ATC code B01AC07.
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