{
  "schema_version": 1,
  "as_of": "2026-09-12",
  "checkpoint_sha256": "0f536a591af59c8ae5ccf2b08d2a1c43804ce23fb94362c6756926789186fe34",
  "scope": "Supplementary factual cross-source context. It does not replace a blank source field or approve a trial connection.",
  "records": [
    {
      "target": {
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        "kind": "rds",
        "brand": "Yesafili",
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        "normalized_sha256": "80b00fe6a05c0bbc350e49f857e082ce746bdfae468a4cfc9cea9fb8378902d8",
        "acquired_at": "2026-09-10T07:34:27.874Z",
        "parser_version": "dhpp-html-v9",
        "source_url": "https://dhpp.hpfb-dgpsa.ca/review-documents/resource/RDS1758225540975",
        "dins": [
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        ]
      },
      "target_decision_date_required": "",
      "selected_din_required": "02535858",
      "submission_control_required": "259183",
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          "value": "Date of Decision: "
        },
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          "value": "Drug Identification Number(s) Issued: 02535858"
        },
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        }
      ],
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        "acquired_at": "2026-09-10T06:22:33.642Z",
        "parser_version": "dhpp-html-v9",
        "source_url": "https://dhpp.hpfb-dgpsa.ca/review-documents/resource/SBD1755873445495",
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      "support_pointers": [
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          "value": "Drug Identification Number (DIN): DIN 02535858 – aflibercept 2 mg/0.05 mL, solution, intravitreal administration"
        },
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        },
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        },
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        },
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          "value": "NDS # 259183  2022-03-16  Issued NOC 2025-06-26  NOC issued for the New Drug Submission. "
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        },
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      ],
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        "kind": "notice_of_compliance",
        "basis": "same_original_nds_control_and_exact_din_in_retained_sbd"
      },
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      "presentation_boundary": "Do not attach the separate SNDS 291460 prefilled-syringe DIN 02558238 event to DIN 02535858. That source row has its own identity.",
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