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BUPROPION HYDROCHLORIDE

NDC 59651-512, BUPROPION HYDROCHLORIDE, tablet, film coated, extended release, from Aurobindo Pharma Limited.

Product NDC
59651-512
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216051
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-512 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE300 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
59651-512-0559651051205500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-512-05)
59651-512-305965105123030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-512-30)
59651-512-905965105129090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-512-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cc344f7c-0eb3-4e63-a09e-b682acca2bb5

Use it

Look up 59651-512 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-512 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-512. 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.