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United States · US · US:71335-2023_6f8dec1e-7fea-454b-99c7-4e3543647336
CARVEDILOL
Orange BookUNIISPLATC C07AG02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeC07AG02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc117133520231100 TABLET, FILM COATED in 1 BOTTLE (71335-2023-1)
- ndc11713352023230 TABLET, FILM COATED in 1 BOTTLE (71335-2023-2)
- ndc11713352023390 TABLET, FILM COATED in 1 BOTTLE (71335-2023-3)
- ndc11713352023460 TABLET, FILM COATED in 1 BOTTLE (71335-2023-4)
- ndc117133520235120 TABLET, FILM COATED in 1 BOTTLE (71335-2023-5)
- ndc117133520236180 TABLET, FILM COATED in 1 BOTTLE (71335-2023-6)
- ndc11713352023710 TABLET, FILM COATED in 1 BOTTLE (71335-2023-7)
Annotations
UNII (FDA Substance ID)
0K47UL67F2
CARVEDILOL
RxCUI 20352
Orange Book
A078165
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0K47UL67F2",
"rxcui": "20352",
"inchikey": "OGHNVEJMJSYVRP-UHFFFAOYSA-N",
"display_name": "CARVEDILOL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"52bd1d20-08ba-1e5e-e063-6294a90ae8a9": {
"match": "brand_token",
"title": "CARVEDILOL TABLET, FILM COATED [COUPLER LLC]",
"spl_version": "1",
"published_date": "2026-05-28"
}
},
"productid": "71335-2023_6f8dec1e-7fea-454b-99c7-4e3543647336",
"productndc": "71335-2023",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "078165",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "3.125MG",
"product_no": "001",
"approval_date": "Sep 5, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "6.25MG",
"product_no": "002",
"approval_date": "Sep 5, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "12.5MG",
"product_no": "003",
"approval_date": "Sep 5, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "004",
"approval_date": "Sep 5, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CARVEDILOL",
"proprietary_name": "CARVEDILOL",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078165",
"marketing_category": "ANDA",
"nonproprietary_name": "CARVEDILOL",
"start_marketing_date": "20210729",
"active_numerator_strength": "25"
}Related drugs
Other records sharing ATC code C07AG02.
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