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Bupropion Hydrochloride SR

NDC 51655-115, bupropion hydrochloride, tablet, extended release, from Northwind Health Company, LLC.

Product NDC
51655-115
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211347
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-115 \
  -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
51655-115-255165501152560 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-25)
51655-115-265165501152690 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-26)
51655-115-525165501155230 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-52)
51655-115-8351655011583180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f2b3939b-a410-6354-e053-2995a90ababb

Use it

Look up 51655-115 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-115 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-115. 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.