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United States · US · US:71335-1545_b6e60516-209f-4738-ade3-6a8c1baf8205
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
- ndc11713351545130 TABLET, FILM COATED in 1 BOTTLE (71335-1545-1)
- ndc11713351545260 TABLET, FILM COATED in 1 BOTTLE (71335-1545-2)
- ndc117133515453100 TABLET, FILM COATED in 1 BOTTLE (71335-1545-3)
- ndc11713351545490 TABLET, FILM COATED in 1 BOTTLE (71335-1545-4)
- ndc117133515455120 TABLET, FILM COATED in 1 BOTTLE (71335-1545-5)
- ndc117133515456180 TABLET, FILM COATED in 1 BOTTLE (71335-1545-6)
- ndc11713351545710 TABLET, FILM COATED in 1 BOTTLE (71335-1545-7)
Annotations
UNII (FDA Substance ID)
0K47UL67F2
CARVEDILOL
RxCUI 20352
Orange Book
A077614
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": "71335-1545_b6e60516-209f-4738-ade3-6a8c1baf8205",
"productndc": "71335-1545",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "077614",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "6.25MG",
"product_no": "001",
"approval_date": "Sep 5, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "12.5MG",
"product_no": "002",
"approval_date": "Sep 5, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "003",
"approval_date": "Sep 5, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "3.125MG",
"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": "ANDA077614",
"marketing_category": "ANDA",
"nonproprietary_name": "Carvedilol",
"start_marketing_date": "20070905",
"active_numerator_strength": "12.5"
}Related drugs
Other records sharing ATC code C07AG02.
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