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United States · US · US:60687-887_40d197a4-871c-104b-e063-6394a90a69fe
Nadolol
Orange BookUNIISPLATC C07AA12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmerican Health Packaging
CountryUS (United States)
ATC codeC07AA12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11606878872130 BLISTER PACK in 1 CARTON (60687-887-21) / 1 TABLET in 1 BLISTER PACK (60687-887-11)
Annotations
UNII (FDA Substance ID)
FEN504330V
NADOLOL
RxCUI 7226
Orange Book
A210955
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": "60687-887_40d197a4-871c-104b-e063-6394a90a69fe",
"productndc": "60687-887",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "210955",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "001",
"approval_date": "Jul 23, 2018"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "40MG",
"product_no": "002",
"approval_date": "Jul 23, 2018"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "80MG",
"product_no": "003",
"approval_date": "Jul 23, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NADOLOL",
"proprietary_name": "Nadolol",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210955",
"marketing_category": "ANDA",
"nonproprietary_name": "Nadolol",
"start_marketing_date": "20251009",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code C07AA12.
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