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Bupropion Hydrochloride

NDC 47335-954, Bupropion Hydrochloride, tablet, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-954
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200695
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-954 \
  -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
47335-954-1347335095413500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-13)
47335-954-814733509548190 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-81)
47335-954-834733509548330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e4e38abf-ef67-405b-af2d-3d8e4533654d

Use it

Look up 47335-954 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-954 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-954. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

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