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Bupropion Hydrochloride SR

NDC 70518-3787, bupropion hydrochloride, tablet, film coated, extended release, from REMEDYREPACK INC..

Product NDC
70518-3787
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205794
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3787 \
  -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
70518-3787-17051837870130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3787-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c76f2f9f-3999-4bdd-8ec3-e0066318d378

Use it

Look up 70518-3787 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3787 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3787. 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.