Back to search
🇺🇸

United States · US · US:71335-0801_645edeba-9a73-4d0a-ac84-2de98e89b760

bupropion

Orange BookUNIISPLATC N06AX12

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN06AX12
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7133508011
    60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-1)
  • ndc11
    7133508012
    180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-2)
  • ndc11
    7133508013
    30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-3)
  • ndc11
    7133508014
    90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-4)
  • ndc11
    7133508015
    120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-5)
  • ndc11
    7133508016
    28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-6)

Annotations

UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
A202304
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": "71335-0801_645edeba-9a73-4d0a-ac84-2de98e89b760",
  "productndc": "71335-0801",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "202304",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "100MG",
        "product_no": "001",
        "approval_date": "May 26, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "150MG",
        "product_no": "002",
        "approval_date": "May 26, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB1",
        "strength": "200MG",
        "product_no": "003",
        "approval_date": "May 26, 2015"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BUPROPION HYDROCHLORIDE",
  "proprietary_name": "bupropion",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202304",
  "marketing_category": "ANDA",
  "nonproprietary_name": "bupropion hydrochloride",
  "start_marketing_date": "20141101",
  "active_numerator_strength": "200"
}

Related drugs

Other records sharing ATC code N06AX12.

Access this data programmatically

Query bupropion 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.