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Bupropion hydrochloride

NDC 71335-2400, Bupropion hydrochloride, tablet, extended release, from Bryant Ranch Prepack.

Product NDC
71335-2400
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216800
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2400 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE200 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
71335-2400-17133524000160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-1)
71335-2400-271335240002180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-2)
71335-2400-37133524000330 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-3)
71335-2400-47133524000490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-4)
71335-2400-571335240005120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-5)
71335-2400-67133524000628 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2400-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5c111cf0-0199-4a4d-8138-81579af4c14d

Use it

Look up 71335-2400 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2400 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2400. 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.