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United States · US · US:69097-917_c1d5cac6-7ca2-4b55-90c3-5ef51df0a1ee

bupropion Hydrochloride

Orange BookUNIISPLATC N06AX12

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

Identification

ManufacturerCIPLA USA INC.,
CountryUS (United States)
ATC codeN06AX12
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    6909791702
    30 TABLET in 1 BOTTLE (69097-917-02)
  • ndc11
    6909791707
    100 TABLET in 1 BOTTLE (69097-917-07)
  • ndc11
    6909791715
    1000 TABLET in 1 BOTTLE (69097-917-15)

Annotations

UNII (FDA Substance ID)
ZG7E5POY8O
BUPROPION HYDROCHLORIDE
RxCUI 203204
Orange Book
A207389
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": "69097-917_c1d5cac6-7ca2-4b55-90c3-5ef51df0a1ee",
  "productndc": "69097-917",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "207389",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "75MG",
        "product_no": "001",
        "approval_date": "Sep 18, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Sep 18, 2017"
      }
    ],
    "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": "ANDA207389",
  "marketing_category": "ANDA",
  "nonproprietary_name": "bupropion Hydrochloride",
  "start_marketing_date": "20180526",
  "active_numerator_strength": "75"
}

Related drugs

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