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Bupropion hydrochloride

NDC 82804-296, Bupropion hydrochloride, tablet, extended release, from Proficient Rx LP.

Product NDC
82804-296
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215568
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82804-296 \
  -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
82804-296-308280402963030 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-296-30)
82804-296-908280402969090 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-296-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f1703bfd-be36-4fde-8e67-df0fb5d93369

Use it

Look up 82804-296 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-296 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-296. 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.