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Bupropion Hydrochloride SR

NDC 42806-413, bupropion hydrochloride, tablet, film coated, extended release, from Epic Pharma, LLC.

Product NDC
42806-413
Status
Listed
Labeler
Epic Pharma, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216766
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42806-413 \
  -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
42806-413-604280604136060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-413-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f56ccdb1-f9d9-3e5f-e053-2995a90a8f16

  • NADAC price for package 42806041360

    GET /v1/drugs/nadac/42806041360

Use it

Look up 42806-413 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42806-413 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42806-413. 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.