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
- 71335-3017_b1f1a5dd-7f53-4ac4-aee3-0a64203c3db3
- Product NDC
- 71335-3017
- Form
- CAPSULE
- Composition / generic term
- phentermine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170124
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENTERMINE HYDROCHLORIDE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (71335-3017-1) · 71335-3017-1
- 42 CAPSULE in 1 BOTTLE (71335-3017-2) · 71335-3017-2
- 14 CAPSULE in 1 BOTTLE (71335-3017-3) · 71335-3017-3
- 20 CAPSULE in 1 BOTTLE (71335-3017-4) · 71335-3017-4
- 28 CAPSULE in 1 BOTTLE (71335-3017-5) · 71335-3017-5
- 60 CAPSULE in 1 BOTTLE (71335-3017-6) · 71335-3017-6
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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