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United States · US · US:46708-404_0bd202e3-c673-4945-b828-1a5bc6a896ae
NADOLOL
Orange BookUNIISPLATC C07AA12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlembic Pharmaceuticals Limited
CountryUS (United States)
ATC codeC07AA12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11467084043030 TABLET in 1 BOTTLE (46708-404-30)
- ndc114670840431100 TABLET in 1 BOTTLE (46708-404-31)
- ndc1146708404911000 TABLET in 1 BOTTLE (46708-404-91)
Annotations
UNII (FDA Substance ID)
FEN504330V
NADOLOL
RxCUI 7226
Orange Book
A211763
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": "46708-404_0bd202e3-c673-4945-b828-1a5bc6a896ae",
"productndc": "46708-404",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "211763",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "001",
"approval_date": "Jun 2, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "40MG",
"product_no": "002",
"approval_date": "Jun 2, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "80MG",
"product_no": "003",
"approval_date": "Jun 2, 2023"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NADOLOL",
"proprietary_name": "NADOLOL",
"active_ingred_unit": "mg/1",
"application_number": "ANDA211763",
"marketing_category": "ANDA",
"nonproprietary_name": "NADOLOL",
"start_marketing_date": "20230608",
"active_numerator_strength": "80"
}Related drugs
Other records sharing ATC code C07AA12.
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