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Bupropion Hydrochloride

NDC 69292-601, Bupropion Hydrochloride, tablet, film coated, from Amici Pharma, Inc..

Product NDC
69292-601
Status
Listed
Labeler
Amici Pharma, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075584
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69292-601 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE75 mg/1

Pharmacologic classes

Aminoketone [EPC]; Dopamine Uptake Inhibitors [MoA]; Increased Dopamine Activity [PE]; Increased Norepinephrine Activity [PE]; Norepinephrine Uptake Inhibitors [MoA]

Package NDCNDC-11Package
69292-601-0169292060101100 TABLET, FILM COATED in 1 BOTTLE (69292-601-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fbb587fa-75c0-4f4d-8eaf-f0e7ba8b5c75

Use it

Look up 69292-601 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69292-601 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69292-601. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.