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Bupropion Hydrochloride

NDC 72789-070, Bupropion Hydrochloride, tablet, film coated, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-070
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/72789-070 \
  -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
72789-070-307278900703030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)
72789-070-907278900709090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/867d3876-6974-4e89-bc45-9e60e84b401c

Use it

Look up 72789-070 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-070 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-070. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.