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United States · US · US:76420-663_0ea9692e-7d75-80f3-e063-6294a90ad6f9

Alprazolam

Orange BookUNIISPLATC N05BA12

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

Identification

ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeN05BA12
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    7642066301
    100 TABLET in 1 BOTTLE (76420-663-01)
  • ndc11
    7642066330
    30 TABLET in 1 BOTTLE (76420-663-30)
  • ndc11
    7642066360
    60 TABLET in 1 BOTTLE (76420-663-60)
  • ndc11
    7642066390
    90 TABLET in 1 BOTTLE (76420-663-90)

Annotations

UNII (FDA Substance ID)
YU55MQ3IZY
ALPRAZOLAM
RxCUI 596
Orange Book
N018276
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "YU55MQ3IZY",
    "rxcui": "596",
    "inchikey": "VREFGVBLTWBCJP-UHFFFAOYSA-N",
    "display_name": "ALPRAZOLAM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "68d8b8d1-00a4-42c4-a796-90211fee1a6d": {
      "match": "brand_token",
      "title": "ALPRAZOLAM TABLET [BRYANT RANCH PREPACK]",
      "spl_version": "104",
      "published_date": "2026-05-22"
    }
  },
  "productid": "76420-663_0ea9692e-7d75-80f3-e063-6294a90ad6f9",
  "productndc": "76420-663",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "018276",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "0.25MG",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "0.5MG",
        "product_no": "002",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "1MG",
        "product_no": "003",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "2MG",
        "product_no": "004",
        "approval_date": "Nov 27, 1985"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": "CIV",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ALPRAZOLAM",
  "proprietary_name": "Alprazolam",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA018276",
  "marketing_category": "NDA AUTHORIZED GENERIC",
  "nonproprietary_name": "alprazolam",
  "start_marketing_date": "19811016",
  "active_numerator_strength": "1"
}

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