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
- 17224-907_338a1502-f356-5e2d-e063-6294a90a5e3e
- Product NDC
- 17224-907
- Form
- TABLET
- Composition / generic term
- PHENTERMINE HYDROCHLORIDE
- Labeler
- Calvin Scott & Co., Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240215
- Source listing expiry
- 20261231
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 (17224-907-07) · 17224-907-07
- 14 TABLET in 1 BOTTLE (17224-907-14) · 17224-907-14
- 28 TABLET in 1 BOTTLE (17224-907-28) · 17224-907-28
- 30 TABLET in 1 BOTTLE (17224-907-30) · 17224-907-30
- 42 TABLET in 1 BOTTLE (17224-907-42) · 17224-907-42
- 45 TABLET in 1 BOTTLE (17224-907-45) · 17224-907-45
- 56 TABLET in 1 BOTTLE (17224-907-56) · 17224-907-56
- 60 TABLET in 1 BOTTLE (17224-907-60) · 17224-907-60
- 84 TABLET in 1 BOTTLE (17224-907-84) · 17224-907-84
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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