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 · 7

ndc11
7133501821
60 TABLET, FILM COATED in 1 BOTTLE (71335-0182-1)
ndc11
7133501822
30 TABLET, FILM COATED in 1 BOTTLE (71335-0182-2)
ndc11
7133501823
100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3)
ndc11
7133501824
90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4)
ndc11
7133501825
120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5)
ndc11
7133501826
15 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6)
ndc11
7133501827
21 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7)

Annotations

UNII (FDA Substance ID)

ZG7E5POY8O

BUPROPION HYDROCHLORIDE

RxCUI 203204

Orange Book

A076143

ABAB

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": "71335-0182_a3743344-f956-4c63-985a-9aaaeeaad923",
  "productndc": "71335-0182",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "076143",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "75MG",
        "product_no": "001",
        "approval_date": "Jan 17, 2006"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Jan 17, 2006"
      }
    ],
    "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": "ANDA076143",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Bupropion Hydrochloride",
  "start_marketing_date": "20060117",
  "active_numerator_strength": "100"
}

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