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Bupropion Hydrochloride (XL)

NDC 80425-0539, bupropion hydrochloride, tablet, film coated, extended release, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0539
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
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/80425-0539 \
  -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
80425-0539-18042505390130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-1)
80425-0539-28042505390260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-2)
80425-0539-38042505390390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3d826804-6427-aae1-e063-6394a90a6593

Use it

Look up 80425-0539 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0539 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0539. 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.