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 · 6

ndc11
7133512141
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-1)
ndc11
7133512142
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-2)
ndc11
7133512143
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-3)
ndc11
7133512144
120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-4)
ndc11
7133512145
8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-5)
ndc11
7133512146
180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6)

Annotations

UNII (FDA Substance ID)

ZG7E5POY8O

BUPROPION HYDROCHLORIDE

RxCUI 203204

Orange Book

A210497

AB3AB3

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": "71335-1214_4e5c9883-8fbd-443f-a356-b0793cd27687",
  "productndc": "71335-1214",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "210497",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB3",
        "strength": "150MG",
        "product_no": "001",
        "approval_date": "Oct 31, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB3",
        "strength": "300MG",
        "product_no": "002",
        "approval_date": "Oct 31, 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": "ANDA210497",
  "marketing_category": "ANDA",
  "nonproprietary_name": "BUPROPION HYDROCHLORIDE",
  "start_marketing_date": "20190325",
  "active_numerator_strength": "300"
}

Related drugs

Other records sharing ATC code N06AX12.

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