Skip to content
healthcare.dev
Get a free key

bupropion hydrochloride SR

NDC 42708-205, bupropion hydrochloride, tablet, film coated, extended release, from QPharma Inc.

Product NDC
42708-205
Status
Listed
Labeler
QPharma Inc
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202304
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-205 \
  -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
42708-205-604270802056060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42708-205-60)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5d6c996e-8965-921c-e063-6394a90abb4e

Use it

Look up 42708-205 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-205 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-205. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Get a free keyNDC docsConnect the MCP server

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.