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United States · US · US:70010-203_4ec654e4-0bd5-934d-e063-6294a90a218d

Sertraline hydrochloride

Orange BookUNIISPLATC N06AB06

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

Identification

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

Packs · 7

  • ndc11
    7001020303
    30 TABLET, FILM COATED in 1 BOTTLE (70010-203-03)
  • ndc11
    7001020305
    500 TABLET, FILM COATED in 1 BOTTLE (70010-203-05)
  • ndc11
    7001020309
    90 TABLET, FILM COATED in 1 BOTTLE (70010-203-09)
  • ndc11
    7001020310
    1000 TABLET, FILM COATED in 1 BOTTLE (70010-203-10)
  • ndc11
    7001020350
    50 TABLET, FILM COATED in 1 BOTTLE (70010-203-50)
  • ndc11
    7001020353
    3000 TABLET, FILM COATED in 1 BOTTLE (70010-203-53)
  • ndc11
    7001020363
    8 BLISTER PACK in 1 CARTON (70010-203-63) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
UTI8907Y6X
SERTRALINE HYDROCHLORIDE
RxCUI 155137
Orange Book
A078403
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": "70010-203_4ec654e4-0bd5-934d-e063-6294a90a218d",
  "productndc": "70010-203",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078403",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE",
        "product_no": "001",
        "approval_date": "Jan 8, 2008"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE",
        "product_no": "002",
        "approval_date": "Jan 8, 2008"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 100MG BASE",
        "product_no": "003",
        "approval_date": "Jan 8, 2008"
      }
    ],
    "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": "ANDA078403",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Sertraline hydrochloride",
  "start_marketing_date": "20230515",
  "active_numerator_strength": "25"
}

Related drugs

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