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
7133518371
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-1)
ndc11
7133518372
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-2)
ndc11
7133518373
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-3)
ndc11
7133518374
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-4)
ndc11
7133518375
45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-5)
ndc11
7133518376
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-6)
ndc11
7133518377
28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-7)
ndc11
7133518378
56 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-8)
ndc11
7133518379
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1837-9)

Annotations

UNII (FDA Substance ID)

ZG7E5POY8O

BUPROPION HYDROCHLORIDE

RxCUI 203204

Orange Book

A211347

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": "71335-1837_baf029ae-b819-465b-82e9-82167b132b79",
  "productndc": "71335-1837",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "211347",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "100MG",
        "product_no": "001",
        "approval_date": "Oct 16, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "150MG",
        "product_no": "002",
        "approval_date": "Oct 16, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "200MG",
        "product_no": "003",
        "approval_date": "Oct 16, 2018"
      }
    ],
    "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": "ANDA211347",
  "marketing_category": "ANDA",
  "nonproprietary_name": "bupropion hydrochloride",
  "start_marketing_date": "20201102",
  "active_numerator_strength": "150"
}

Related drugs

Other records sharing ATC code N06AX12.

Access this data programmatically

Query Bupropion Hydrochloride and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs