Amoxapine

Orange BookUNIISPLATC N06AA17

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerActavis Pharma, Inc.

CountryUS (United States)

ATC codeN06AA17

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0591571301
100 TABLET in 1 BOTTLE, PLASTIC (0591-5713-01)

Annotations

UNII (FDA Substance ID)

R63VQ857OT

AMOXAPINE

RxCUI 722

Orange Book

A072691

ABABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "R63VQ857OT",
    "rxcui": "722",
    "inchikey": "QWGDMFLQWFTERH-UHFFFAOYSA-N",
    "display_name": "AMOXAPINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a16297df-3158-48db-85e5-5cd506885556": {
      "match": "brand_token",
      "title": "AMOXAPINE TABLET [ACTAVIS PHARMA, INC.]",
      "spl_version": "20",
      "published_date": "2026-02-23"
    }
  },
  "productid": "0591-5713_40931661-1155-4850-baaa-227f066ed616",
  "productndc": "0591-5713",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "072691",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "001",
        "approval_date": "Aug 28, 1992"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "002",
        "approval_date": "Aug 28, 1992"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "003",
        "approval_date": "Aug 28, 1992"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "004",
        "approval_date": "Aug 28, 1992"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "AMOXAPINE",
  "proprietary_name": "Amoxapine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA072691",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Amoxapine",
  "start_marketing_date": "19920828",
  "active_numerator_strength": "25"
}

Related drugs

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