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United States · US · US:68788-7539_336e6f60-39b9-4997-b697-873dca01c65f

Carvedilol

Orange BookUNIISPLATC C07AG02

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerPreferred Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeC07AG02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6878875391
    100 TABLET, FILM COATED in 1 BOTTLE (68788-7539-1)
  • ndc11
    6878875393
    30 TABLET, FILM COATED in 1 BOTTLE (68788-7539-3)
  • ndc11
    6878875396
    60 TABLET, FILM COATED in 1 BOTTLE (68788-7539-6)
  • ndc11
    6878875399
    90 TABLET, FILM COATED in 1 BOTTLE (68788-7539-9)

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": "68788-7539_336e6f60-39b9-4997-b697-873dca01c65f",
  "productndc": "68788-7539",
  "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"
}

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