Nortriptyline Hydrochloride

Orange BookUNIISPLATC N06AA10

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AA10

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
7133500832
60 CAPSULE in 1 BOTTLE (71335-0083-2)
ndc11
7133500834
30 CAPSULE in 1 BOTTLE (71335-0083-4)
ndc11
7133500835
90 CAPSULE in 1 BOTTLE (71335-0083-5)
ndc11
7133500836
50 CAPSULE in 1 BOTTLE (71335-0083-6)
ndc11
7133500837
100 CAPSULE in 1 BOTTLE (71335-0083-7)
ndc11
7133500838
120 CAPSULE in 1 BOTTLE (71335-0083-8)
ndc11
7133500839
28 CAPSULE in 1 BOTTLE (71335-0083-9)

Annotations

UNII (FDA Substance ID)

00FN6IH15D

NORTRIPTYLINE HYDROCHLORIDE

RxCUI 203130

Orange Book

A075520

ABABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "00FN6IH15D",
    "rxcui": "203130",
    "inchikey": "SHAYBENGXDALFF-UHFFFAOYSA-N",
    "display_name": "NORTRIPTYLINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "21770082-7a99-520d-e063-6394a90ab9cb": {
      "match": "brand_token",
      "title": "NORTRIPTYLINE HYDROCHLORIDE CAPSULE [ST. MARY'S MEDICAL PARK PHARMACY]",
      "spl_version": "4",
      "published_date": "2026-05-21"
    }
  },
  "productid": "71335-0083_1c7ab195-2d22-4021-9af0-f77317695c7c",
  "productndc": "71335-0083",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "075520",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE",
        "product_no": "001",
        "approval_date": "May 8, 2000"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 75MG BASE",
        "product_no": "002",
        "approval_date": "May 8, 2000"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE",
        "product_no": "003",
        "approval_date": "May 8, 2000"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "004",
        "approval_date": "May 8, 2000"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NORTRIPTYLINE HYDROCHLORIDE",
  "proprietary_name": "Nortriptyline Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075520",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Nortriptyline Hydrochloride",
  "start_marketing_date": "20000508",
  "active_numerator_strength": "25"
}

Related drugs

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