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United States · US · US:65862-157_19f7a08f-58bd-45b8-a750-4432ae161455

Paroxetine

Orange BookSPL

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

Identification

ManufacturerAurobindo Pharma Limited
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    6586215701
    100 TABLET, FILM COATED in 1 BOTTLE (65862-157-01)
  • ndc11
    6586215705
    500 TABLET, FILM COATED in 1 BOTTLE (65862-157-05)
  • ndc11
    6586215730
    30 TABLET, FILM COATED in 1 BOTTLE (65862-157-30)
  • ndc11
    6586215790
    90 TABLET, FILM COATED in 1 BOTTLE (65862-157-90)
  • ndc11
    6586215799
    1000 TABLET, FILM COATED in 1 BOTTLE (65862-157-99)

Annotations

Orange Book
A078406
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "ORAL",
  "spl_meta": {
    "e63fe922-b35a-406c-8737-f3f5e6d5a30d": {
      "match": "brand_token",
      "title": "PAROXETINE (PAROXETINE HYDROCHLORIDE) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]",
      "spl_version": "17",
      "published_date": "2026-06-01"
    }
  },
  "productid": "65862-157_19f7a08f-58bd-45b8-a750-4432ae161455",
  "productndc": "65862-157",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078406",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "001",
        "approval_date": "Jul 25, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "002",
        "approval_date": "Jul 25, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 30MG BASE",
        "product_no": "003",
        "approval_date": "Jul 25, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "004",
        "approval_date": "Jul 25, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE",
  "proprietary_name": "Paroxetine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078406",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Paroxetine Hydrochloride",
  "start_marketing_date": "20070725",
  "active_numerator_strength": "40"
}

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