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
- 17224-730_2f21c9dc-8661-1aa1-e063-6394a90ac697
- Product NDC
- 17224-730
- Form
- TABLET
- Composition / generic term
- DIETHYLPROPION HYDROCHLORIDE
- Labeler
- Calvin Scott & Co., Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101227
- Source listing expiry
- 20261231
Source-listed ingredients
- DIETHYLPROPION HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 28 TABLET in 1 BOTTLE, PLASTIC (17224-730-28) · 17224-730-28
- 30 TABLET in 1 BOTTLE, PLASTIC (17224-730-30) · 17224-730-30
- 56 TABLET in 1 BOTTLE, PLASTIC (17224-730-56) · 17224-730-56
- 60 TABLET in 1 BOTTLE, PLASTIC (17224-730-60) · 17224-730-60
- 84 TABLET in 1 BOTTLE, PLASTIC (17224-730-84) · 17224-730-84
- 90 TABLET in 1 BOTTLE, PLASTIC (17224-730-90) · 17224-730-90
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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