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United States · US · US:50090-7561_819dc63a-621e-4db4-866c-11c84160585d
Atenolol
Orange BookUNIISPLATC C07AB03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeC07AB03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11500907561090 TABLET in 1 BOTTLE (50090-7561-0)
Annotations
UNII (FDA Substance ID)
50VV3VW0TI
ATENOLOL
RxCUI 1202
Orange Book
A213136
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": "50090-7561_819dc63a-621e-4db4-866c-11c84160585d",
"productndc": "50090-7561",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "213136",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Nov 21, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Nov 21, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "100MG",
"product_no": "003",
"approval_date": "Nov 21, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ATENOLOL",
"proprietary_name": "Atenolol",
"active_ingred_unit": "mg/1",
"application_number": "ANDA213136",
"marketing_category": "ANDA",
"nonproprietary_name": "Atenolol",
"start_marketing_date": "20191121",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code C07AB03.
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