Paroxetine

Orange BookSPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerYiling Pharmaceutical, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
6911700271
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-1)
ndc11
6911700272
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-2)
ndc11
6911700273
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-3)
ndc11
6911700274
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-4)
ndc11
6911700275
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-5)

Annotations

Orange Book

A211248

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": "69117-0027_472863af-ee04-24a6-e063-6394a90a9e20",
  "productndc": "69117-0027",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "211248",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "001",
        "approval_date": "Nov 2, 2021"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "002",
        "approval_date": "Nov 2, 2021"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 30MG BASE",
        "product_no": "003",
        "approval_date": "Nov 2, 2021"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 40MG BASE",
        "product_no": "004",
        "approval_date": "Nov 2, 2021"
      }
    ],
    "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": "ANDA211248",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Paroxetine",
  "start_marketing_date": "20211102",
  "active_numerator_strength": "40"
}

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