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BUPROPION HYDROCHLORIDE

NDC 80425-0461, BUPROPION HYDROCHLORIDE, tablet, extended release, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0461
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210497
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0461 \
  -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
80425-0461-18042504610130 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-1)
80425-0461-28042504610260 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-2)
80425-0461-38042504610390 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0461-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/29a6c6e3-f30f-6541-e063-6394a90ae11d

Use it

Look up 80425-0461 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0461 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0461. 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.