{
 "drug": "Pindolol Tablet",
 "asOf": "2026-08-25",
 "status": "discontinuing",
 "since": "01/30/2026",
 "dayN": 207,
 "cat": "Cardiovascular",
 "companies": [
  "Sun Pharmaceutical Industries, Inc."
 ],
 "reasons": [],
 "records": [
  {
   "discontinued_date": "01/30/2026",
   "update_type": "New",
   "initial_posting_date": "01/30/2026",
   "package_ndc": "57664-656-88",
   "generic_name": "Pindolol Tablet",
   "contact_info": "800-818-4555",
   "related_info": "Discontinuation of the manufacture of the drug; Expiry date of last distributed batch October 2026",
   "openfda": {
    "application_number": [
     "ANDA074063"
    ],
    "brand_name": [
     "PINDOLOL"
    ],
    "generic_name": [
     "PINDOLOL"
    ],
    "manufacturer_name": [
     "Sun Pharmaceutical Industries, Inc."
    ],
    "product_ndc": [
     "57664-656",
     "57664-655"
    ],
    "product_type": [
     "HUMAN PRESCRIPTION DRUG"
    ],
    "route": [
     "ORAL"
    ],
    "substance_name": [
     "PINDOLOL"
    ],
    "rxcui": [
     "198104",
     "198105"
    ],
    "spl_id": [
     "4d3c89dd-e947-5f23-e063-6294a90aeb1f"
    ],
    "spl_set_id": [
     "b331a73f-bf7b-4442-8901-36d016530279"
    ],
    "package_ndc": [
     "57664-656-88",
     "57664-655-88"
    ],
    "nui": [
     "N0000000161",
     "N0000175556"
    ],
    "pharm_class_moa": [
     "Adrenergic beta-Antagonists [MoA]"
    ],
    "pharm_class_epc": [
     "beta-Adrenergic Blocker [EPC]"
    ],
    "unii": [
     "BJ4HF6IU1D"
    ]
   },
   "update_date": "01/30/2026",
   "therapeutic_category": [
    "Cardiovascular"
   ],
   "dosage_form": "Tablet",
   "presentation": "Pindolol, Tablet, 10 mg (NDC 57664-656-88)",
   "company_name": "Sun Pharmaceutical Industries, Inc.",
   "status": "To Be Discontinued"
  },
  {
   "discontinued_date": "01/30/2026",
   "update_type": "New",
   "initial_posting_date": "01/30/2026",
   "package_ndc": "57664-655-88",
   "generic_name": "Pindolol Tablet",
   "contact_info": "800-818-4555",
   "related_info": "Discontinuation of the manufacture of the drug; Expiry date of last distributed batch January 2027",
   "openfda": {
    "application_number": [
     "ANDA074063"
    ],
    "brand_name": [
     "PINDOLOL"
    ],
    "generic_name": [
     "PINDOLOL"
    ],
    "manufacturer_name": [
     "Sun Pharmaceutical Industries, Inc."
    ],
    "product_ndc": [
     "57664-655",
     "57664-656"
    ],
    "product_type": [
     "HUMAN PRESCRIPTION DRUG"
    ],
    "route": [
     "ORAL"
    ],
    "substance_name": [
     "PINDOLOL"
    ],
    "rxcui": [
     "198104",
     "198105"
    ],
    "spl_id": [
     "4d3c89dd-e947-5f23-e063-6294a90aeb1f"
    ],
    "spl_set_id": [
     "b331a73f-bf7b-4442-8901-36d016530279"
    ],
    "package_ndc": [
     "57664-656-88",
     "57664-655-88"
    ],
    "nui": [
     "N0000000161",
     "N0000175556"
    ],
    "pharm_class_moa": [
     "Adrenergic beta-Antagonists [MoA]"
    ],
    "pharm_class_epc": [
     "beta-Adrenergic Blocker [EPC]"
    ],
    "unii": [
     "BJ4HF6IU1D"
    ]
   },
   "update_date": "01/30/2026",
   "therapeutic_category": [
    "Cardiovascular"
   ],
   "dosage_form": "Tablet",
   "presentation": "Pindolol, Tablet, 5 mg (NDC 57664-655-88)",
   "company_name": "Sun Pharmaceutical Industries, Inc.",
   "status": "To Be Discontinued"
  }
 ]
}