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United States · US · US:71335-0154_23c84f99-953a-4085-b1bd-4bb713a6ac79

ZOLPIDEM TARTRATE

Orange BookUNIISPLATC N05CF02

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN05CF02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133501540
    5 TABLET in 1 BOTTLE (71335-0154-0)
  • ndc11
    7133501541
    30 TABLET in 1 BOTTLE (71335-0154-1)
  • ndc11
    7133501542
    60 TABLET in 1 BOTTLE (71335-0154-2)
  • ndc11
    7133501543
    100 TABLET in 1 BOTTLE (71335-0154-3)
  • ndc11
    7133501544
    50 TABLET in 1 BOTTLE (71335-0154-4)
  • ndc11
    7133501545
    90 TABLET in 1 BOTTLE (71335-0154-5)
  • ndc11
    7133501546
    10 TABLET in 1 BOTTLE (71335-0154-6)
  • ndc11
    7133501547
    15 TABLET in 1 BOTTLE (71335-0154-7)
  • ndc11
    7133501548
    28 TABLET in 1 BOTTLE (71335-0154-8)
  • ndc11
    7133501549
    120 TABLET in 1 BOTTLE (71335-0154-9)

Annotations

UNII (FDA Substance ID)
WY6W63843K
ZOLPIDEM TARTRATE
RxCUI 221183
Orange Book
A077903
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "WY6W63843K",
    "rxcui": "221183",
    "inchikey": "VXRDAMSNTXUHFX-CEAXSRTFSA-N",
    "display_name": "ZOLPIDEM TARTRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "b49f6c18-e155-4728-a79a-9354e8c3c8f4": {
      "match": "brand_token",
      "title": "ZOLPIDEM TARTRATE CAPSULE [UMEDICA LABORATORIES USA INC.]",
      "spl_version": "2",
      "published_date": "2026-05-27"
    }
  },
  "productid": "71335-0154_23c84f99-953a-4085-b1bd-4bb713a6ac79",
  "productndc": "71335-0154",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "077903",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Aug 17, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Aug 17, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIV",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ZOLPIDEM TARTRATE",
  "proprietary_name": "ZOLPIDEM TARTRATE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077903",
  "marketing_category": "ANDA",
  "nonproprietary_name": "zolpidem tartrate",
  "start_marketing_date": "20070905",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code N05CF02.

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