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Benzphetamine Hydrochloride

NDC 42806-081, Benzphetamine Hydrochloride, tablet, film coated, from Epic Pharma, LLC.

Product NDC
42806-081
Status
Listed
Labeler
Epic Pharma, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090346
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42806-081 \
  -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
42806-081-0142806008101100 TABLET, FILM COATED in 1 BOTTLE (42806-081-01)
42806-081-0542806008105500 TABLET, FILM COATED in 1 BOTTLE (42806-081-05)
42806-081-304280600813030 TABLET, FILM COATED in 1 BOTTLE (42806-081-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f6d9b369-4b64-4d3f-844d-5d60dd257c55

Use it

Look up 42806-081 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42806-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42806-081. 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.