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United States · US · US:68180-351_37fc8b27-bf23-4fe6-8d44-5331bde5b466

Sertraline Hydrochloride

Orange BookUNIISPLATC N06AB06

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerLupin Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeN06AB06
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    6818035103
    1000 TABLET, FILM COATED in 1 BOTTLE (68180-351-03)
  • ndc11
    6818035106
    30 TABLET, FILM COATED in 1 BOTTLE (68180-351-06)
  • ndc11
    6818035109
    90 TABLET, FILM COATED in 1 BOTTLE (68180-351-09)

Annotations

UNII (FDA Substance ID)
UTI8907Y6X
SERTRALINE HYDROCHLORIDE
RxCUI 155137
Orange Book
A077670
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": "68180-351_37fc8b27-bf23-4fe6-8d44-5331bde5b466",
  "productndc": "68180-351",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "077670",
    "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": "ANDA077670",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Sertraline Hydrochloride",
  "start_marketing_date": "20070206",
  "active_numerator_strength": "25"
}

Related drugs

Other records sharing ATC code N06AB06.

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