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Bupropion Hydrochloride (XL)

NDC 63629-8476, bupropion hydrochloride, tablet, film coated, extended release, from Bryant Ranch Prepack.

Product NDC
63629-8476
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207479
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63629-8476 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE300 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
63629-8476-16362984760130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-8476-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/96e78f74-fad0-4ae1-9e68-55e4c6ab2d60

Use it

Look up 63629-8476 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63629-8476 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63629-8476. 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.