Duloxetine

Orange BookUNIISPLATC N06AX21

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AX21

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
7133516721
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-1)
ndc11
7133516722
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-2)
ndc11
7133516723
28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-3)
ndc11
7133516724
6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-4)
ndc11
7133516725
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-5)
ndc11
7133516726
15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-6)
ndc11
7133516727
180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-7)
ndc11
7133516728
120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-8)

Annotations

UNII (FDA Substance ID)

9044SC542W

DULOXETINE HYDROCHLORIDE

RxCUI 476250

Orange Book

A203197

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "9044SC542W",
    "rxcui": "476250",
    "inchikey": "BFFSMCNJSOPUAY-LMOVPXPDSA-N",
    "display_name": "DULOXETINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9dab9154-b86f-40dc-a4d1-18e6534dbc78": {
      "match": "brand_token",
      "title": "DULOXETINE CAPSULE, DELAYED RELEASE PELLETS [ACTAVIS PHARMA, INC.]",
      "spl_version": "28",
      "published_date": "2026-05-20"
    }
  },
  "productid": "71335-1672_a5fa1183-35f7-41b9-8452-5d00ccd868a3",
  "productndc": "71335-1672",
  "dosage_form": "CAPSULE, DELAYED RELEASE",
  "orange_book": {
    "appl_no": "203197",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Aug 26, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 30MG BASE",
        "product_no": "002",
        "approval_date": "Aug 26, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 60MG BASE",
        "product_no": "003",
        "approval_date": "Aug 26, 2015"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DULOXETINE HYDROCHLORIDE",
  "proprietary_name": "Duloxetine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA203197",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Duloxetine",
  "start_marketing_date": "20120501",
  "active_numerator_strength": "30"
}

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