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Bupropion Hydrochloride

NDC 71335-0013, Bupropion Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-0013
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-0013 \
  -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
71335-0013-17133500130130 TABLET, FILM COATED in 1 BOTTLE (71335-0013-1)
71335-0013-27133500130260 TABLET, FILM COATED in 1 BOTTLE (71335-0013-2)
71335-0013-37133500130390 TABLET, FILM COATED in 1 BOTTLE (71335-0013-3)
71335-0013-4713350013047 TABLET, FILM COATED in 1 BOTTLE (71335-0013-4)
71335-0013-57133500130514 TABLET, FILM COATED in 1 BOTTLE (71335-0013-5)
71335-0013-671335001306120 TABLET, FILM COATED in 1 BOTTLE (71335-0013-6)
71335-0013-771335001307100 TABLET, FILM COATED in 1 BOTTLE (71335-0013-7)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1d722dc2-7909-454e-b989-095677079044

Use it

Look up 71335-0013 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0013 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0013. 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.