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Bupropion Hydrochloride

NDC 62332-127, Bupropion Hydrochloride, tablet, film coated, from Alembic Pharmaceuticals Inc..

Product NDC
62332-127
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203013
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62332-127 \
  -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
62332-127-3162332012731100 TABLET, FILM COATED in 1 BOTTLE (62332-127-31)
62332-127-7162332012771500 TABLET, FILM COATED in 1 BOTTLE (62332-127-71)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b303a0ad-5971-44ab-937c-bcf3ff650358

  • NADAC price for package 62332012731

    GET /v1/drugs/nadac/62332012731

Use it

Look up 62332-127 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-127 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-127. 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.