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United States · US · US:0575-6200_451aa56d-e2e5-402f-843a-cddb5b3d37dd

Proglycem

Orange BookUNIISPLATC V03AH01

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

Identification

ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC codeV03AH01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0575620030
    1 BOTTLE, DROPPER in 1 BOX (0575-6200-30) / 30 mL in 1 BOTTLE, DROPPER

Annotations

UNII (FDA Substance ID)
O5CB12L4FN
DIAZOXIDE
RxCUI 3327
Orange Book
N017453
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "O5CB12L4FN",
    "rxcui": "3327",
    "inchikey": "GDLBFKVLRPITMI-UHFFFAOYSA-N",
    "display_name": "DIAZOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "b16c7832-2fd9-49af-b923-1dc0d91fd6e2": {
      "match": "brand_token",
      "title": "PROGLYCEM (DIAZOXIDE) SUSPENSION [TEVA PHARMACEUTICALS USA, INC.]",
      "spl_version": "15",
      "published_date": "2024-07-23"
    }
  },
  "productid": "0575-6200_451aa56d-e2e5-402f-843a-cddb5b3d37dd",
  "productndc": "0575-6200",
  "dosage_form": "SUSPENSION",
  "orange_book": {
    "appl_no": "017453",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "50MG/ML",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DIAZOXIDE",
  "proprietary_name": "Proglycem",
  "active_ingred_unit": "mg/mL",
  "application_number": "NDA017453",
  "marketing_category": "NDA",
  "nonproprietary_name": "diazoxide",
  "start_marketing_date": "19900930",
  "active_numerator_strength": "50"
}

Related drugs

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