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
- 11534-160_a9fd0c08-60ae-4015-85c7-803989d00745
- Product NDC
- 11534-160
- Form
- TABLET
- Composition / generic term
- phentermine hydrochloride
- Labeler
- SUNRISE PHARMACEUTICAL, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170124
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENTERMINE HYDROCHLORIDE — 37.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (11534-160-01) · 11534-160-01
- 1000 TABLET in 1 BOTTLE (11534-160-03) · 11534-160-03
- 30 TABLET in 1 BOTTLE (11534-160-30) · 11534-160-30
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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