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Bupropion Hydrochloride XL

NDC 82804-080, bupropion hydrochloride, tablet, extended release, from Proficient Rx LP.

Product NDC
82804-080
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210015
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82804-080 \
  -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
82804-080-308280400803030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-30)
82804-080-608280400806060 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-60)
82804-080-908280400809090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dfd5f264-d4fd-4441-88b1-48086c7c0616

Use it

Look up 82804-080 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-080 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-080. 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.