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
- 71335-0161_098e240a-c834-444a-a56c-933a6a102df5
- Product NDC
- 71335-0161
- Form
- TABLET
- Composition / generic term
- Phentermine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110308
- Source listing expiry
- 20261231
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 (71335-0161-0) · 71335-0161-0
- 30 TABLET in 1 BOTTLE (71335-0161-1) · 71335-0161-1
- 15 TABLET in 1 BOTTLE (71335-0161-2) · 71335-0161-2
- 28 TABLET in 1 BOTTLE (71335-0161-3) · 71335-0161-3
- 7 TABLET in 1 BOTTLE (71335-0161-4) · 71335-0161-4
- 14 TABLET in 1 BOTTLE (71335-0161-5) · 71335-0161-5
- 60 TABLET in 1 BOTTLE (71335-0161-6) · 71335-0161-6
- 45 TABLET in 1 BOTTLE (71335-0161-7) · 71335-0161-7
- 2 TABLET in 1 BOTTLE (71335-0161-8) · 71335-0161-8
- 21 TABLET in 1 BOTTLE (71335-0161-9) · 71335-0161-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →