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United States · US · US:55111-329_4e11dea8-92ab-762e-9808-fad73bf42330

Nateglinide

Orange BookUNIISPLATC A10BX03

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

Identification

ManufacturerDr. Reddy's Laboratories Limited
CountryUS (United States)
ATC codeA10BX03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    5511132901
    100 TABLET in 1 BOTTLE (55111-329-01)
  • ndc11
    5511132905
    500 TABLET in 1 BOTTLE (55111-329-05)
  • ndc11
    5511132930
    30 TABLET in 1 BOTTLE (55111-329-30)
  • ndc11
    5511132978
    10 BLISTER PACK in 1 CARTON (55111-329-78) / 10 TABLET in 1 BLISTER PACK (55111-329-79)
  • ndc11
    5511132990
    90 TABLET in 1 BOTTLE (55111-329-90)

Annotations

UNII (FDA Substance ID)
41X3PWK4O2
NATEGLINIDE
RxCUI 274332
Orange Book
A077461
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "41X3PWK4O2",
    "rxcui": "274332",
    "inchikey": "OELFLUMRDSZNSF-BRWVUGGUSA-N",
    "display_name": "NATEGLINIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "f7b28951-76d2-cabd-64a1-b74aa225c6e9": {
      "match": "brand_token",
      "title": "NATEGLINIDE TABLET [DR. REDDY'S LABORATORIES LIMITED]",
      "spl_version": "11",
      "published_date": "2025-09-01"
    }
  },
  "productid": "55111-329_4e11dea8-92ab-762e-9808-fad73bf42330",
  "productndc": "55111-329",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077461",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "60MG",
        "product_no": "001",
        "approval_date": "Sep 9, 2009"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "120MG",
        "product_no": "002",
        "approval_date": "Sep 9, 2009"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NATEGLINIDE",
  "proprietary_name": "Nateglinide",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077461",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Nateglinide",
  "start_marketing_date": "20090909",
  "active_numerator_strength": "120"
}

Related drugs

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