Sertraline Hydrochloride

Orange BookUNIISPLATC N06AB06

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AB06

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 9

ndc11
7133504031
30 TABLET, FILM COATED in 1 BOTTLE (71335-0403-1)
ndc11
7133504032
60 TABLET, FILM COATED in 1 BOTTLE (71335-0403-2)
ndc11
7133504033
90 TABLET, FILM COATED in 1 BOTTLE (71335-0403-3)
ndc11
7133504034
180 TABLET, FILM COATED in 1 BOTTLE (71335-0403-4)
ndc11
7133504035
100 TABLET, FILM COATED in 1 BOTTLE (71335-0403-5)
ndc11
7133504036
56 TABLET, FILM COATED in 1 BOTTLE (71335-0403-6)
ndc11
7133504037
28 TABLET, FILM COATED in 1 BOTTLE (71335-0403-7)
ndc11
7133504038
120 TABLET, FILM COATED in 1 BOTTLE (71335-0403-8)
ndc11
7133504039
15 TABLET, FILM COATED in 1 BOTTLE (71335-0403-9)

Annotations

UNII (FDA Substance ID)

UTI8907Y6X

SERTRALINE HYDROCHLORIDE

RxCUI 155137

Orange Book

A077206

ABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "UTI8907Y6X",
    "rxcui": "155137",
    "inchikey": "BLFQGGGGFNSJKA-XHXSRVRCSA-N",
    "display_name": "SERTRALINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "6c26a87a-b2b6-4302-bb8d-2031461f28ce": {
      "match": "brand_token",
      "title": "SERTRALINE HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK]",
      "spl_version": "103",
      "published_date": "2026-05-28"
    }
  },
  "productid": "71335-0403_1ec34f1e-b59c-4cff-b867-eb1465506cd1",
  "productndc": "71335-0403",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "077206",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE",
        "product_no": "001",
        "approval_date": "Feb 6, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE",
        "product_no": "002",
        "approval_date": "Feb 6, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 100MG BASE",
        "product_no": "003",
        "approval_date": "Feb 6, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SERTRALINE HYDROCHLORIDE",
  "proprietary_name": "Sertraline Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077206",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Sertraline Hydrochloride",
  "start_marketing_date": "20070206",
  "active_numerator_strength": "50"
}

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