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Bupropion Hydrochloride

NDC 0904-6635, Bupropion Hydrochloride, tablet, film coated, from Major Pharmaceuticals.

Product NDC
0904-6635
Status
Listed
Labeler
Major Pharmaceuticals
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/0904-6635 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE75 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
0904-6635-6100904663561100 BLISTER PACK in 1 CARTON (0904-6635-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b127d3fc-be5e-4c12-8026-205766bf8e7f

  • NADAC price for package 00904663561

    GET /v1/drugs/nadac/00904663561

Use it

Look up 0904-6635 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0904-6635 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0904-6635. 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.