Bupropion hydrochloride

Orange BookUNIISPLATC N06AX12

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AX12

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 9

ndc11
7133524571
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-1)
ndc11
7133524572
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-2)
ndc11
7133524573
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-3)
ndc11
7133524574
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-4)
ndc11
7133524575
45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-5)
ndc11
7133524576
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-6)
ndc11
7133524577
28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-7)
ndc11
7133524578
56 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-8)
ndc11
7133524579
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2457-9)

Annotations

UNII (FDA Substance ID)

ZG7E5POY8O

BUPROPION HYDROCHLORIDE

RxCUI 203204

Orange Book

A216800

AB1AB1AB1

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "ZG7E5POY8O",
    "rxcui": "203204",
    "inchikey": "HEYVINCGKDONRU-UHFFFAOYSA-N",
    "display_name": "BUPROPION HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "cefaaa17-f79a-4ba6-8f97-a59f60e07b75": {
      "match": "brand_token",
      "title": "BUPROPION HYDROCHLORIDE (XL) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]",
      "spl_version": "105",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-2457_8f9001c7-e11f-452a-8bbf-4515d87ec8ed",
  "productndc": "71335-2457",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "216800",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "100MG",
        "product_no": "001",
        "approval_date": "May 31, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "150MG",
        "product_no": "002",
        "approval_date": "May 31, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "200MG",
        "product_no": "003",
        "approval_date": "May 31, 2023"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BUPROPION HYDROCHLORIDE",
  "proprietary_name": "Bupropion hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA216800",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Bupropion hydrochloride",
  "start_marketing_date": "20230531",
  "active_numerator_strength": "150"
}

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