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United States · US · US:71335-2652_f87d9697-16ab-4ea8-9cd8-b6e326407a7d

BUPROPION HYDROCHLORIDE

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 · 7

  • ndc11
    7133526521
    60 TABLET, FILM COATED in 1 BOTTLE (71335-2652-1)
  • ndc11
    7133526522
    30 TABLET, FILM COATED in 1 BOTTLE (71335-2652-2)
  • ndc11
    7133526523
    100 TABLET, FILM COATED in 1 BOTTLE (71335-2652-3)
  • ndc11
    7133526524
    90 TABLET, FILM COATED in 1 BOTTLE (71335-2652-4)
  • ndc11
    7133526525
    120 TABLET, FILM COATED in 1 BOTTLE (71335-2652-5)
  • ndc11
    7133526526
    15 TABLET, FILM COATED in 1 BOTTLE (71335-2652-6)
  • ndc11
    7133526527
    21 TABLET, FILM COATED in 1 BOTTLE (71335-2652-7)

Annotations

UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
A075491
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": "71335-2652_f87d9697-16ab-4ea8-9cd8-b6e326407a7d",
  "productndc": "71335-2652",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "075491",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "75MG",
        "product_no": "001",
        "approval_date": "Apr 17, 2000"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Apr 17, 2000"
      }
    ],
    "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": "ANDA075491",
  "marketing_category": "ANDA",
  "nonproprietary_name": "BUPROPION HYDROCHLORIDE",
  "start_marketing_date": "20240425",
  "active_numerator_strength": "100"
}

Related drugs

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