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Bupropion hydrochloride

NDC 0615-8602, Bupropion hydrochloride, tablet, extended release, from NCS HealthCare of KY, LLC dba Vangard Labs.

Product NDC
0615-8602
Status
Listed
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216800
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8602 \
  -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
0615-8602-390061586023930 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8602-39)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1bd2ed35-35c5-464f-bf51-9dd4b42ee59a

Use it

Look up 0615-8602 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8602 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0615-8602. 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.