Midodrine Hydrochloride

Orange BookUNIISPLATC C01CA17

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

Identification

ManufacturerProficient Rx LP

CountryUS (United States)

ATC codeC01CA17

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
7120590600
100 TABLET in 1 BOTTLE, PLASTIC (71205-906-00)
ndc11
7120590611
1000 TABLET in 1 BOTTLE, PLASTIC (71205-906-11)
ndc11
7120590630
30 TABLET in 1 BOTTLE, PLASTIC (71205-906-30)
ndc11
7120590655
500 TABLET in 1 BOTTLE, PLASTIC (71205-906-55)
ndc11
7120590660
60 TABLET in 1 BOTTLE, PLASTIC (71205-906-60)
ndc11
7120590672
120 TABLET in 1 BOTTLE, PLASTIC (71205-906-72)
ndc11
7120590690
90 TABLET in 1 BOTTLE, PLASTIC (71205-906-90)

Annotations

UNII (FDA Substance ID)

59JV96YTXV

MIDODRINE HYDROCHLORIDE

RxCUI 993491

Orange Book

A207849

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": "71205-906_fac1a712-e714-4137-8604-2ba0f048901c",
  "productndc": "71205-906",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "207849",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "2.5MG",
        "product_no": "001",
        "approval_date": "Oct 1, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "002",
        "approval_date": "Oct 1, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "003",
        "approval_date": "Oct 1, 2020"
      }
    ],
    "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": "ANDA207849",
  "marketing_category": "ANDA",
  "nonproprietary_name": "midodrine hydrochloride",
  "start_marketing_date": "20201015",
  "active_numerator_strength": "10"
}

Related drugs

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