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Bupropion hydrochloride

NDC 47335-736, Bupropion hydrochloride, tablet, film coated, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-736
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078866
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-736 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE100 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
47335-736-0847335073608100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-08)
47335-736-1347335073613500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-13)
47335-736-864733507368660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-86)
47335-736-8847335073688100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-736-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/29848192-7de3-4c0d-a822-1268dcf128b0

Use it

Look up 47335-736 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-736 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-736. 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.