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BUPROPION HYDROCHLORIDE

NDC 70010-125, bupropion hydrochloride, tablet, film coated, extended release, from Granules Pharmaceuticals Inc..

Product NDC
70010-125
Status
Listed
Labeler
Granules Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218385
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70010-125 \
  -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
70010-125-037001001250330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-03)
70010-125-0570010012505500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-05)
70010-125-067001001250660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-125-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/61e9cbe3-8211-42f3-b68f-581f56651919

Use it

Look up 70010-125 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70010-125 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70010-125. 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.