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Bupropion Hydrochloride SR

NDC 43598-536, bupropion hydrochloride, tablet, film coated, extended release, from Dr. Reddy�s Laboratories Inc..

Product NDC
43598-536
Status
Listed
Labeler
Dr. Reddy�s Laboratories Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205794
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-536 \
  -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
43598-536-0143598053601100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-536-01)
43598-536-0543598053605500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-536-05)
43598-536-604359805366060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-536-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6948f63b-599c-4956-a249-e9544beda9fc

Use it

Look up 43598-536 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-536 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-536. 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.