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Bupropion Hydrochloride XL

NDC 60687-782, Bupropion Hydrochloride, tablet, extended release, from American Health Packaging.

Product NDC
60687-782
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090693
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60687-782 \
  -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
60687-782-0160687078201100 BLISTER PACK in 1 CARTON (60687-782-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-782-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8dab6d17-bf41-4a28-90db-b66959c0e143

  • NADAC price for package 60687078201

    GET /v1/drugs/nadac/60687078201

Use it

Look up 60687-782 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-782. 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.