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WELLBUTRIN SR

NDC 0173-0947, bupropion hydrochloride, tablet, film coated, from GlaxoSmithKline LLC.

Product NDC
0173-0947
Status
Listed
Labeler
GlaxoSmithKline LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020358
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0173-0947 \
  -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
0173-0947-550017309475560 TABLET, FILM COATED in 1 BOTTLE (0173-0947-55)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cbc8c074-f080-4489-a5ae-207b5fadeba3

  • NADAC price for package 00173094755

    GET /v1/drugs/nadac/00173094755

Use it

Look up 0173-0947 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0173-0947 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0173-0947. 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.