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BENZPHETAMINE HYDROCHLORIDE

NDC 10702-040, benzphetamine hydrochloride, tablet, from KVK-TECH, INC.

Product NDC
10702-040
Status
Listed
Labeler
KVK-TECH, 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/10702-040 \
  -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
10702-040-0110702004001100 TABLET in 1 BOTTLE (10702-040-01)
10702-040-031070200400330 TABLET in 1 BOTTLE (10702-040-03)
10702-040-10107020040101000 TABLET in 1 BOTTLE (10702-040-10)
10702-040-5010702004050500 TABLET in 1 BOTTLE (10702-040-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/14d4589d-7f1c-4b6e-9557-59dad39b0960

Use it

Look up 10702-040 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-040 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-040. 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.