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Bupropion Hydrochloride (XL)

NDC 68788-4172, bupropion hydrochloride, tablet, film coated, extended release, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4172
Status
Listed
Labeler
Preferred 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/68788-4172 \
  -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
68788-4172-168788417201100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-4172-1)
68788-4172-36878841720330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-4172-3)
68788-4172-66878841720660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-4172-6)
68788-4172-868788417208120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-4172-8)
68788-4172-96878841720990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-4172-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/30c370c2-f2b7-4335-ba55-e8c8f4059092

Use it

Look up 68788-4172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4172. 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.