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Bupropion Hydrochloride

NDC 60760-781, Bupropion Hydrochloride, tablet, film coated, from St. Mary's Medical Park Pharmacy.

Product NDC
60760-781
Status
Listed
Labeler
St. Mary's Medical Park Pharmacy
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/60760-781 \
  -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
60760-781-306076007813030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-781-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/362504fd-2f0a-c097-e063-6394a90ac0fc

Use it

Look up 60760-781 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60760-781 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60760-781. 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.