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
- 71335-0451_98aa03d7-8df0-4b01-8371-9761a0176afa
- Product NDC
- 71335-0451
- Form
- TABLET
- Composition / generic term
- benzphetamine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100721
- 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 (71335-0451-1) · 71335-0451-1
- 7 TABLET in 1 BOTTLE (71335-0451-2) · 71335-0451-2
- 14 TABLET in 1 BOTTLE (71335-0451-3) · 71335-0451-3
- 21 TABLET in 1 BOTTLE (71335-0451-4) · 71335-0451-4
- 42 TABLET in 1 BOTTLE (71335-0451-5) · 71335-0451-5
- 84 TABLET in 1 BOTTLE (71335-0451-6) · 71335-0451-6
- 60 TABLET in 1 BOTTLE (71335-0451-7) · 71335-0451-7
- 90 TABLET in 1 BOTTLE (71335-0451-8) · 71335-0451-8
- 120 TABLET in 1 BOTTLE (71335-0451-9) · 71335-0451-9
Source and coverage
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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.
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