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
- 68071-3400_2d54077e-4c8e-aaae-e063-6394a90adb41
- Product NDC
- 68071-3400
- Form
- TABLET
- Composition / generic term
- DIETHYLPROPION HYDROCHLORIDE
- Labeler
- NuCare Pharmaceuticals,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
- 112 TABLET in 1 BOTTLE (68071-3400-0) · 68071-3400-0
- 21 TABLET in 1 BOTTLE (68071-3400-1) · 68071-3400-1
- 42 TABLET in 1 BOTTLE (68071-3400-2) · 68071-3400-2
- 30 TABLET in 1 BOTTLE (68071-3400-3) · 68071-3400-3
- 84 TABLET in 1 BOTTLE (68071-3400-4) · 68071-3400-4
- 56 TABLET in 1 BOTTLE (68071-3400-5) · 68071-3400-5
- 14 TABLET in 1 BOTTLE (68071-3400-7) · 68071-3400-7
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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