United States · FDA National Drug Code directory
Diethylpropion 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
- 71335-0175_76b09c8e-b98d-4f3b-a200-29883379bdfe
- Product NDC
- 71335-0175
- Form
- TABLET
- Composition / generic term
- Diethylpropion Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110718
- Source listing expiry
- 20261231
Source-listed ingredients
- DIETHYLPROPION HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 42 TABLET in 1 BOTTLE (71335-0175-0) · 71335-0175-0
- 28 TABLET in 1 BOTTLE (71335-0175-1) · 71335-0175-1
- 90 TABLET in 1 BOTTLE (71335-0175-2) · 71335-0175-2
- 30 TABLET in 1 BOTTLE (71335-0175-3) · 71335-0175-3
- 14 TABLET in 1 BOTTLE (71335-0175-4) · 71335-0175-4
- 21 TABLET in 1 BOTTLE (71335-0175-5) · 71335-0175-5
- 7 TABLET in 1 BOTTLE (71335-0175-6) · 71335-0175-6
- 60 TABLET in 1 BOTTLE (71335-0175-7) · 71335-0175-7
- 84 TABLET in 1 BOTTLE (71335-0175-8) · 71335-0175-8
- 56 TABLET in 1 BOTTLE (71335-0175-9) · 71335-0175-9
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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