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United States · US · US:68071-3138_0ec45c14-def9-b2b9-e063-6294a90a3a3a

Carvedilol

Orange BookUNIISPLATC C07AG02

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

Identification

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

Packs · 4

  • ndc11
    6807131383
    30 TABLET, FILM COATED in 1 BOTTLE (68071-3138-3)
  • ndc11
    6807131386
    60 TABLET, FILM COATED in 1 BOTTLE (68071-3138-6)
  • ndc11
    6807131388
    180 TABLET, FILM COATED in 1 BOTTLE (68071-3138-8)
  • ndc11
    6807131389
    90 TABLET, FILM COATED in 1 BOTTLE (68071-3138-9)

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": "68071-3138_0ec45c14-def9-b2b9-e063-6294a90a3a3a",
  "productndc": "68071-3138",
  "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": "3.125"
}

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