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Bupropion Hydrochloride (XL)

NDC 77771-145, bupropion hydrochloride, tablet, film coated, extended release, from RADHA PHARMACEUTICALS, INC..

Product NDC
77771-145
Status
Listed
Labeler
RADHA PHARMACEUTICALS, 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/77771-145 \
  -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
77771-145-0577771014505500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-145-05)
77771-145-307777101453030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-145-30)
77771-145-907777101459090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-145-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/16a788ff-8bd5-4f70-a3fd-a89db019e435

Use it

Look up 77771-145 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/77771-145 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 77771-145. 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.