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
7133502101
30 TABLET, FILM COATED in 1 BOTTLE (71335-0210-1)
ndc11
7133502102
60 TABLET, FILM COATED in 1 BOTTLE (71335-0210-2)
ndc11
7133502103
90 TABLET, FILM COATED in 1 BOTTLE (71335-0210-3)
ndc11
7133502104
180 TABLET, FILM COATED in 1 BOTTLE (71335-0210-4)
ndc11
7133502105
28 TABLET, FILM COATED in 1 BOTTLE (71335-0210-5)
ndc11
7133502106
15 TABLET, FILM COATED in 1 BOTTLE (71335-0210-6)
ndc11
7133502107
120 TABLET, FILM COATED in 1 BOTTLE (71335-0210-7)
ndc11
7133502108
100 TABLET, FILM COATED in 1 BOTTLE (71335-0210-8)
ndc11
7133502109
45 TABLET, FILM COATED in 1 BOTTLE (71335-0210-9)

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": "71335-0210_f1cfc28f-bd82-4ffe-b413-5ef9d140a86f",
  "productndc": "71335-0210",
  "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": "100"
}

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