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United States · US · US:69097-869_39a5df9f-6bc8-480f-84a6-d051d2cef465
Nadolol
Orange BookUNIISPLATC C07AA12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCipla USA Inc.
CountryUS (United States)
ATC codeC07AA12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11690978690230 TABLET in 1 BOTTLE (69097-869-02)
- ndc116909786907100 TABLET in 1 BOTTLE (69097-869-07)
- ndc1169097869151000 TABLET in 1 BOTTLE (69097-869-15)
Annotations
UNII (FDA Substance ID)
FEN504330V
NADOLOL
RxCUI 7226
Orange Book
A203455
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "FEN504330V",
"rxcui": "7226",
"inchikey": "VWPOSFSPZNDTMJ-UCWKZMIHSA-N",
"display_name": "NADOLOL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c154d99c-e4fb-41d0-8fac-e1982672e8d7": {
"match": "brand_token",
"title": "NADOLOL TABLET [BRYANT RANCH PREPACK]",
"spl_version": "103",
"published_date": "2026-06-01"
}
},
"productid": "69097-869_39a5df9f-6bc8-480f-84a6-d051d2cef465",
"productndc": "69097-869",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "203455",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "001",
"approval_date": "Dec 18, 2015"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "40MG",
"product_no": "002",
"approval_date": "Dec 18, 2015"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "80MG",
"product_no": "003",
"approval_date": "Dec 18, 2015"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NADOLOL",
"proprietary_name": "Nadolol",
"active_ingred_unit": "mg/1",
"application_number": "ANDA203455",
"marketing_category": "ANDA",
"nonproprietary_name": "Nadolol",
"start_marketing_date": "20160223",
"active_numerator_strength": "80"
}Related drugs
Other records sharing ATC code C07AA12.
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