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Bupropion Hydrochloride (XL)

NDC 50090-7335, bupropion hydrochloride, tablet, film coated, extended release, from A-S Medication Solutions.

Product NDC
50090-7335
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207479
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7335 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE300 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
50090-7335-05009073350090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7335-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0ac739de-ad59-4882-810e-f52db22ac96f

Use it

Look up 50090-7335 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7335 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7335. 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.