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United States · US · US:71610-651_a189f92d-a14a-45be-8f55-4b81fe2dce92

SERTRALINE HYDROCHLORIDE

Orange BookUNIISPLATC N06AB06

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

Identification

ManufacturerAphena Pharma Solutions - Tennessee, LLC
CountryUS (United States)
ATC codeN06AB06
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    7161065115
    15 TABLET, FILM COATED in 1 BOTTLE (71610-651-15)
  • ndc11
    7161065130
    30 TABLET, FILM COATED in 1 BOTTLE (71610-651-30)
  • ndc11
    7161065145
    45 TABLET, FILM COATED in 1 BOTTLE (71610-651-45)
  • ndc11
    7161065153
    60 TABLET, FILM COATED in 1 BOTTLE (71610-651-53)
  • ndc11
    7161065160
    90 TABLET, FILM COATED in 1 BOTTLE (71610-651-60)
  • ndc11
    7161065173
    135 TABLET, FILM COATED in 1 BOTTLE (71610-651-73)
  • ndc11
    7161065180
    180 TABLET, FILM COATED in 1 BOTTLE (71610-651-80)

Annotations

UNII (FDA Substance ID)
UTI8907Y6X
SERTRALINE HYDROCHLORIDE
RxCUI 155137
Orange Book
A202825
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": "71610-651_a189f92d-a14a-45be-8f55-4b81fe2dce92",
  "productndc": "71610-651",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "202825",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE",
        "product_no": "001",
        "approval_date": "Nov 7, 2014"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE",
        "product_no": "002",
        "approval_date": "Nov 7, 2014"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 100MG BASE",
        "product_no": "003",
        "approval_date": "Nov 7, 2014"
      }
    ],
    "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": "ANDA202825",
  "marketing_category": "ANDA",
  "nonproprietary_name": "SERTRALINE HYDROCHLORIDE",
  "start_marketing_date": "20170209",
  "active_numerator_strength": "100"
}

Related drugs

Other records sharing ATC code N06AB06.

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