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United States · US · US:42708-012_45b43876-f7b3-e3e8-e063-6394a90ad40a
Atenolol
Orange BookUNIISPLATC C07AB03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerQPharma, Inc.
CountryUS (United States)
ATC codeC07AB03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11427080123030 TABLET in 1 BOTTLE (42708-012-30)
Annotations
UNII (FDA Substance ID)
50VV3VW0TI
ATENOLOL
RxCUI 1202
Orange Book
A074056
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": "42708-012_45b43876-f7b3-e3e8-e063-6394a90ad40a",
"productndc": "42708-012",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "074056",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "001",
"approval_date": "Jan 18, 1995"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "100MG",
"product_no": "002",
"approval_date": "Jan 18, 1995"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "003",
"approval_date": "Jul 19, 2004"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ATENOLOL",
"proprietary_name": "Atenolol",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074056",
"marketing_category": "ANDA",
"nonproprietary_name": "Atenolol",
"start_marketing_date": "19950222",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code C07AB03.
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