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BUPROPION HYDROCHLORIDE

NDC 50090-7511, BUPROPION HYDROCHLORIDE, tablet, film coated, from A-S Medication Solutions.

Product NDC
50090-7511
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075491
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7511 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE100 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
50090-7511-05009075110060 TABLET, FILM COATED in 1 BOTTLE (50090-7511-0)
50090-7511-35009075110390 TABLET, FILM COATED in 1 BOTTLE (50090-7511-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d86e26e0-6e10-4d59-8cc8-94b551774b86

Use it

Look up 50090-7511 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7511 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7511. 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.