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Bupropion hydrochloride

NDC 68788-4010, Bupropion hydrochloride, tablet, extended release, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4010
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215568
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4010 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPROPION HYDROCHLORIDE150 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
68788-4010-168788401001100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4010-1)
68788-4010-36878840100330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4010-3)
68788-4010-66878840100660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4010-6)
68788-4010-96878840100990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4010-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/069e6828-e599-4614-9645-9cf1382ac93e

Use it

Look up 68788-4010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4010. 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.