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bupropion hydrochloride

NDC 70518-4674, bupropion hydrochloride, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-4674
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211020
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4674 \
  -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
70518-4674-07051846740030 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4674-0)
70518-4674-17051846740190 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4674-1)
70518-4674-27051846740230 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4674-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/136f29fa-a859-4efb-8365-1382716d6f8f

Use it

Look up 70518-4674 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4674 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4674. 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.