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United States · US · US:60505-1325_ef40d4d7-e3ab-70fd-f7a0-b9c02055f734

Midodrine Hydrochloride

Orange BookUNIISPLATC C01CA17

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

Identification

ManufacturerApotex Corp
CountryUS (United States)
ATC codeC01CA17
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6050513251
    100 TABLET in 1 BOTTLE (60505-1325-1)
  • ndc11
    6050513253
    30 TABLET in 1 BOTTLE (60505-1325-3)
  • ndc11
    6050513255
    500 TABLET in 1 BOTTLE (60505-1325-5)
  • ndc11
    6050513258
    1000 TABLET in 1 BOTTLE (60505-1325-8)

Annotations

UNII (FDA Substance ID)
59JV96YTXV
MIDODRINE HYDROCHLORIDE
RxCUI 993491
Orange Book
A077746
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "59JV96YTXV",
    "rxcui": "993491",
    "inchikey": "MGCQZNBCJBRZDT-UHFFFAOYSA-N",
    "display_name": "MIDODRINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4d5e42be-3476-85d4-e063-6294a90a0865": {
      "match": "brand_token",
      "title": "MIDODRINE HYDROCHLORIDE TABLET [AVET PHARMACEUTICALS INC.]",
      "spl_version": "1",
      "published_date": "2026-03-27"
    }
  },
  "productid": "60505-1325_ef40d4d7-e3ab-70fd-f7a0-b9c02055f734",
  "productndc": "60505-1325",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077746",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "001",
        "approval_date": "Sep 12, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "002",
        "approval_date": "Sep 12, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "003",
        "approval_date": "Sep 12, 2006"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "MIDODRINE HYDROCHLORIDE",
  "proprietary_name": "Midodrine Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077746",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Midodrine Hydrochloride",
  "start_marketing_date": "20060912",
  "active_numerator_strength": "10"
}

Related drugs

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