United States · FDA National Drug Code directory

benzphetamine hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 17224-672_f5ee265f-9765-de77-e053-2a95a90ac76f
Product NDC: 17224-672
Form: TABLET
Composition / generic term: BENZPHETAMINE HYDROCHLORIDE
Labeler: Calvin Scott & Co., Inc.
Marketing category: ANDA
Marketing start / end (source format): 20100101
Source listing expiry: 20261231

Source-listed ingredients

BENZPHETAMINE HYDROCHLORIDE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE, PLASTIC (17224-672-30) · 17224-672-30
60 TABLET in 1 BOTTLE, PLASTIC (17224-672-60) · 17224-672-60

Source and coverage

Open FDA National Drug Code directory →

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →