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United States · US · US:71335-2774_12063fb8-2fa7-472a-b32c-ea41f77acbcf

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 · 7

  • ndc11
    7133527741
    100 TABLET in 1 BOTTLE (71335-2774-1)
  • ndc11
    7133527742
    30 TABLET in 1 BOTTLE (71335-2774-2)
  • ndc11
    7133527743
    60 TABLET in 1 BOTTLE (71335-2774-3)
  • ndc11
    7133527744
    90 TABLET in 1 BOTTLE (71335-2774-4)
  • ndc11
    7133527745
    20 TABLET in 1 BOTTLE (71335-2774-5)
  • ndc11
    7133527746
    180 TABLET in 1 BOTTLE (71335-2774-6)
  • ndc11
    7133527747
    10 TABLET in 1 BOTTLE (71335-2774-7)

Annotations

UNII (FDA Substance ID)
50VV3VW0TI
ATENOLOL
RxCUI 1202
Orange Book
A213136
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": "71335-2774_12063fb8-2fa7-472a-b32c-ea41f77acbcf",
  "productndc": "71335-2774",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "213136",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Nov 21, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "002",
        "approval_date": "Nov 21, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Nov 21, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ATENOLOL",
  "proprietary_name": "Atenolol",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA213136",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Atenolol",
  "start_marketing_date": "20191121",
  "active_numerator_strength": "100"
}

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