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Bupropion Hydrochloride

NDC 0115-6811, BUPROPION HYDROCHLORIDE, tablet, film coated, extended release, from Amneal Pharmaceuticals of New York LLC.

Product NDC
0115-6811
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
ANDA077415
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0115-6811 \
  -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
0115-6811-0200115681102500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-02)
0115-6811-080011568110830 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-08)
0115-6811-100011568111090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fddc9630-2f9a-4104-888f-3714587d4fe7

Use it

Look up 0115-6811 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0115-6811 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0115-6811. 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.