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United States · US · US:68071-3851_426703da-1cb8-fb58-e063-6394a90abdec
Atenolol
Orange BookUNIISPLATC C07AB03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals,Inc.
CountryUS (United States)
ATC codeC07AB03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11680713851330 TABLET in 1 BOTTLE (68071-3851-3)
- ndc11680713851660 TABLET in 1 BOTTLE (68071-3851-6)
- ndc11680713851990 TABLET in 1 BOTTLE (68071-3851-9)
Annotations
UNII (FDA Substance ID)
50VV3VW0TI
ATENOLOL
RxCUI 1202
Orange Book
A078512
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": "68071-3851_426703da-1cb8-fb58-e063-6394a90abdec",
"productndc": "68071-3851",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "078512",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Oct 31, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Oct 31, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "100MG",
"product_no": "003",
"approval_date": "Oct 31, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ATENOLOL",
"proprietary_name": "Atenolol",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078512",
"marketing_category": "ANDA",
"nonproprietary_name": "Atenolol",
"start_marketing_date": "20071031",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code C07AB03.
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