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Bupropion Hydrochloride (XL)

NDC 43598-656, bupropion hydrochloride, tablet, film coated, extended release, from Dr Reddys Laboratories Inc.

Product NDC
43598-656
Status
Listed
Labeler
Dr Reddys Laboratories Inc
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207479
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-656 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE300 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
43598-656-0543598065605500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-05)
43598-656-304359806563030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-30)
43598-656-904359806569090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d5469d64-5e74-4b7a-b4cd-551665f6adaa

  • NADAC price for package 43598065605

    GET /v1/drugs/nadac/43598065605

  • NADAC price for package 43598065630

    GET /v1/drugs/nadac/43598065630

Use it

Look up 43598-656 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-656 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-656. 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.