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Bupropion Hydrochloride

NDC 70518-4218, Bupropion Hydrochloride, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-4218
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203013
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4218 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE100 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
70518-4218-07051842180030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4218-0)
70518-4218-17051842180190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4218-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/990587bd-4c7d-4a36-8a38-3104648ab3a2

Use it

Look up 70518-4218 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4218 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4218. 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.