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Bupropion Hydrochloride

NDC 68001-309, Bupropion Hydrochloride, tablet, film coated, from BluePoint Laboratories.

Product NDC
68001-309
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076143
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-309 \
  -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
68001-309-0068001030900100 TABLET, FILM COATED in 1 BOTTLE (68001-309-00)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7d035056-44ab-444d-9d27-125b3f571140

  • NADAC price for package 68001030900

    GET /v1/drugs/nadac/68001030900

Use it

Look up 68001-309 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-309 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-309. 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.