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Bupropion Hydrochloride (SR)

NDC 33342-528, Bupropion Hydrochloride, tablet, extended release, from Macleods Pharmaceuticals Limited.

Product NDC
33342-528
Status
Listed
Labeler
Macleods Pharmaceuticals Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218567
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/33342-528 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE200 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
33342-528-093334205280960 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-528-09)
33342-528-1133342052811100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-528-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6127b24e-261c-4b64-8423-ebe583676abe

Use it

Look up 33342-528 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/33342-528 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 33342-528. 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.