United States · FDA National Drug Code directory
Phentermine 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
- 17224-901_4a195805-16d2-9214-e063-6394a90ac691
- Product NDC
- 17224-901
- Form
- TABLET
- Composition / generic term
- PHENTERMINE HYDROCHLORIDE
- Labeler
- Calvin Scott & Co., Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130812
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENTERMINE HYDROCHLORIDE — 37.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 TABLET in 1 BOTTLE, PLASTIC (17224-901-07) · 17224-901-07
- 14 TABLET in 1 BOTTLE, PLASTIC (17224-901-14) · 17224-901-14
- 28 TABLET in 1 BOTTLE, PLASTIC (17224-901-28) · 17224-901-28
- 30 TABLET in 1 BOTTLE, PLASTIC (17224-901-30) · 17224-901-30
- 45 TABLET in 1 BOTTLE, PLASTIC (17224-901-45) · 17224-901-45
- 60 TABLET in 1 BOTTLE, PLASTIC (17224-901-60) · 17224-901-60
- 90 TABLET in 1 BOTTLE, PLASTIC (17224-901-90) · 17224-901-90
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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