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bupropion hydrochloride SR

NDC 55154-0183, bupropion hydrochloride, tablet, film coated, extended release, from Cardinal Health 107, LLC.

Product NDC
55154-0183
Status
Listed
Labeler
Cardinal Health 107, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202304
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55154-0183 \
  -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
55154-0183-05515401830010 BLISTER PACK in 1 BAG (55154-0183-0) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/439a7e93-f578-434f-943f-4b93c35450f5

Use it

Look up 55154-0183 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55154-0183 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55154-0183. 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.