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United States · US · US:52427-430_ecd0de7b-801e-a5d6-01b7-01b89a8f3a78
TENORMIN
Orange BookUNIISPLATC C07AB03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlmatica Pharma LLC
CountryUS (United States)
ATC codeC07AB03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11524274309090 TABLET in 1 BOTTLE (52427-430-90)
Annotations
UNII (FDA Substance ID)
50VV3VW0TI
ATENOLOL
RxCUI 1202
Orange Book
N018240
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": {
"6e850b1e-28a4-4ff8-8ed7-bb0b29faa28a": {
"match": "brand_token",
"title": "TENORMIN (ATENOLOL) TABLET [UPSHER-SMITH LABORATORIES, LLC]",
"spl_version": "2",
"published_date": "2026-05-01"
}
},
"productid": "52427-430_ecd0de7b-801e-a5d6-01b7-01b89a8f3a78",
"productndc": "52427-430",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "018240",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "50MG",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "100MG",
"product_no": "002",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "25MG",
"product_no": "004",
"approval_date": "Apr 9, 1990"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ATENOLOL",
"proprietary_name": "TENORMIN",
"active_ingred_unit": "mg/1",
"application_number": "NDA018240",
"marketing_category": "NDA",
"nonproprietary_name": "Atenolol",
"start_marketing_date": "20150415",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code C07AB03.
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