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Bupropion Hydrochloride (XL)

NDC 76282-480, bupropion hydrochloride, tablet, extended release, from Exelan Pharmaceuticals Inc..

Product NDC
76282-480
Status
Listed
Labeler
Exelan Pharmaceuticals Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206556
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76282-480 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE150 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
76282-480-0576282048005500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-480-05)
76282-480-307628204803030 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-480-30)
76282-480-907628204809090 TABLET, EXTENDED RELEASE in 1 BOTTLE (76282-480-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8a0781c0-e7d5-498e-b7d3-d6bd457f175f

Use it

Look up 76282-480 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76282-480 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76282-480. 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.