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United States · US · US:71335-1616_984af795-bb5a-4156-b2cd-09707d12b5a2

Atenolol

Orange BookUNIISPLATC C07AB03

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeC07AB03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7133516161
    30 TABLET in 1 BOTTLE (71335-1616-1)
  • ndc11
    7133516162
    100 TABLET in 1 BOTTLE (71335-1616-2)
  • ndc11
    7133516163
    60 TABLET in 1 BOTTLE (71335-1616-3)
  • ndc11
    7133516164
    90 TABLET in 1 BOTTLE (71335-1616-4)
  • ndc11
    7133516165
    20 TABLET in 1 BOTTLE (71335-1616-5)
  • ndc11
    7133516166
    180 TABLET in 1 BOTTLE (71335-1616-6)

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": "71335-1616_984af795-bb5a-4156-b2cd-09707d12b5a2",
  "productndc": "71335-1616",
  "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": "20041116",
  "active_numerator_strength": "25"
}

Related drugs

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