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Bupropion Hydrochloride

NDC 76420-812, Bupropion Hydrochloride, tablet, extended release, from Asclemed USA, Inc..

Product NDC
76420-812
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077285
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-812 \
  -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
76420-812-0176420081201100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-01)
76420-812-0576420081205500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-05)
76420-812-307642008123030 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-30)
76420-812-607642008126060 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-60)
76420-812-907642008129090 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-812-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/637e89e5-8f6e-4392-8045-a778cb9ed138

Use it

Look up 76420-812 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-812 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-812. 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.