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Bupropion Hydrochloride

NDC 0115-5445, BUPROPION HYDROCHLORIDE, tablet, film coated, extended release, from Amneal Pharmaceuticals of New York LLC.

Product NDC
0115-5445
Status
Listed
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076711
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0115-5445 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE200 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
0115-5445-130011554451360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-5445-13)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e962fb9a-d9fb-49c5-a8b4-0b355b8f829b

Use it

Look up 0115-5445 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0115-5445 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0115-5445. 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.