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United States · US · US:72664-212_05f81151-3c12-9235-e063-6294a90af890
NADOLOL
Orange BookUNIISPLATC C07AA12
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerVGYAAN Pharmaceuticals LLC
CountryUS (United States)
ATC codeC07AA12
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc117266421201100 TABLET in 1 BOTTLE, PLASTIC (72664-212-01)
Annotations
UNII (FDA Substance ID)
FEN504330V
NADOLOL
RxCUI 7226
Orange Book
A212856
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": "72664-212_05f81151-3c12-9235-e063-6294a90af890",
"productndc": "72664-212",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "212856",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "001",
"approval_date": "Sep 13, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "40MG",
"product_no": "002",
"approval_date": "Sep 13, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "80MG",
"product_no": "003",
"approval_date": "Sep 13, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NADOLOL",
"proprietary_name": "NADOLOL",
"active_ingred_unit": "mg/1",
"application_number": "ANDA212856",
"marketing_category": "ANDA",
"nonproprietary_name": "NADOLOL",
"start_marketing_date": "20200630",
"active_numerator_strength": "40"
}Related drugs
Other records sharing ATC code C07AA12.
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