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
- 71335-3107_1a792fd4-4ba0-458d-90d1-b5dde6a5934a
- Product NDC
- 71335-3107
- Form
- TABLET
- 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 — 37.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (71335-3107-0) · 71335-3107-0
- 30 TABLET in 1 BOTTLE (71335-3107-1) · 71335-3107-1
- 15 TABLET in 1 BOTTLE (71335-3107-2) · 71335-3107-2
- 28 TABLET in 1 BOTTLE (71335-3107-3) · 71335-3107-3
- 7 TABLET in 1 BOTTLE (71335-3107-4) · 71335-3107-4
- 14 TABLET in 1 BOTTLE (71335-3107-5) · 71335-3107-5
- 60 TABLET in 1 BOTTLE (71335-3107-6) · 71335-3107-6
- 45 TABLET in 1 BOTTLE (71335-3107-7) · 71335-3107-7
- 2 TABLET in 1 BOTTLE (71335-3107-8) · 71335-3107-8
- 21 TABLET in 1 BOTTLE (71335-3107-9) · 71335-3107-9
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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