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Bupropion Hydrochloride XL

NDC 71205-291, Bupropion Hydrochloride, tablet, extended release, from Proficient Rx LP.

Product NDC
71205-291
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207224
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-291 \
  -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
71205-291-307120502913030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-30)
71205-291-607120502916060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-60)
71205-291-907120502919090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5e568bb5-542a-4395-a21e-dc64281d694e

Use it

Look up 71205-291 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-291 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-291. 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.