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benzphetamine hydrochloride

NDC 17224-672, BENZPHETAMINE HYDROCHLORIDE, tablet, from Calvin Scott & Co., Inc..

Product NDC
17224-672
Status
Listed
Labeler
Calvin Scott & Co., Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090968
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17224-672 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENZPHETAMINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Appetite Suppression [PE]; Increased Sympathetic Activity [PE]; Sympathomimetic Amine Anorectic [EPC]

Package NDCNDC-11Package
17224-672-301722406723030 TABLET in 1 BOTTLE, PLASTIC (17224-672-30)
17224-672-601722406726060 TABLET in 1 BOTTLE, PLASTIC (17224-672-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f5c3c2ed-54a2-1def-e053-2995a90ab4e3

Use it

Look up 17224-672 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17224-672 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17224-672. 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.