Miochol E

Orange Book

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBausch & Lomb Incorporated

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
2420853920
1 KIT in 1 BLISTER PACK (24208-539-20) * 2 mL in 1 VIAL * 2 mL in 1 AMPULE

Annotations

Orange Book

N020213

Raw payload (JSON)

{
  "route": null,
  "productid": "24208-539_19c42ee4-9f98-48da-85ea-52090070c2e2",
  "productndc": "24208-539",
  "dosage_form": "KIT",
  "orange_book": {
    "appl_no": "020213",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "20MG/VIAL",
        "product_no": "001",
        "approval_date": "Sep 22, 1993"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": null,
  "proprietary_name": "Miochol E",
  "active_ingred_unit": null,
  "application_number": "NDA020213",
  "marketing_category": "NDA",
  "nonproprietary_name": "acetylcholine chloride",
  "start_marketing_date": "19930922",
  "active_numerator_strength": null
}

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