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United States · US · US:0615-8372_df64fdd3-c7fc-46aa-9691-ae2a44453280
Atenolol
Orange BookUNIISPLATC C07AB03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
CountryUS (United States)
ATC codeC07AB03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11061583720515 TABLET in 1 BLISTER PACK (0615-8372-05)
- ndc11061583723930 TABLET in 1 BLISTER PACK (0615-8372-39)
Annotations
UNII (FDA Substance ID)
50VV3VW0TI
ATENOLOL
RxCUI 1202
Orange Book
A077443
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "50VV3VW0TI",
"rxcui": "1202",
"inchikey": "METKIMKYRPQLGS-UHFFFAOYSA-N",
"display_name": "ATENOLOL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"2ee7b7da-303d-4a57-a1eb-25e8923660c0": {
"match": "brand_token",
"title": "ATENOLOL TABLET [ASCLEMED USA INC.]",
"spl_version": "1",
"published_date": "2026-05-21"
}
},
"productid": "0615-8372_df64fdd3-c7fc-46aa-9691-ae2a44453280",
"productndc": "0615-8372",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "077443",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Sep 13, 2006"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Sep 13, 2006"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "100MG",
"product_no": "003",
"approval_date": "Sep 13, 2006"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ATENOLOL",
"proprietary_name": "Atenolol",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077443",
"marketing_category": "ANDA",
"nonproprietary_name": "Atenolol",
"start_marketing_date": "20100610",
"active_numerator_strength": "25"
}Related drugs
Other records sharing ATC code C07AB03.
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