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United States · US · US:49884-250_d4b26d87-0345-449f-88c1-2d6a9eefd699

Olanzapine and Fluoxetine

Orange BookUNIISPLATC N06AB

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

Identification

ManufacturerPar Health USA, LLC
CountryUS (United States)
ATC codeN06AB
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    4988425011
    30 CAPSULE in 1 BOTTLE, PLASTIC (49884-250-11)

Annotations

UNII (FDA Substance ID)
I9W7N6B1KJ
FLUOXETINE HYDROCHLORIDE
RxCUI 227224
Orange Book
A077742
ABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "I9W7N6B1KJ",
    "rxcui": "227224",
    "inchikey": "GIYXAJPCNFJEHY-UHFFFAOYSA-N",
    "display_name": "FLUOXETINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "52b99337-afa8-a6f9-e063-6294a90a2038": {
      "match": "brand_token",
      "title": "OLANZAPINE TABLET, FILM COATED [COUPLER LLC]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "49884-250_d4b26d87-0345-449f-88c1-2d6a9eefd699",
  "productndc": "49884-250",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "077742",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE;EQ 3MG BASE",
        "product_no": "001",
        "approval_date": "Nov 2, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE;EQ 6MG BASE",
        "product_no": "002",
        "approval_date": "Nov 2, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE;EQ 12MG BASE",
        "product_no": "003",
        "approval_date": "Nov 2, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE;EQ 6MG BASE",
        "product_no": "004",
        "approval_date": "Nov 2, 2012"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE;EQ 12MG BASE",
        "product_no": "005",
        "approval_date": "Nov 2, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "FLUOXETINE HYDROCHLORIDE; OLANZAPINE",
  "proprietary_name": "Olanzapine and Fluoxetine",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "ANDA077742",
  "marketing_category": "ANDA",
  "nonproprietary_name": "olanzapine and fuoxetine",
  "start_marketing_date": "20121126",
  "active_numerator_strength": "25; 6"
}

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