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
- 71335-0350_abbf6752-a400-4afe-9550-b4eb0ba7687c
- Product NDC
- 71335-0350
- Form
- TABLET
- Composition / generic term
- Phentermine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130812
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENTERMINE HYDROCHLORIDE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (71335-0350-0) · 71335-0350-0
- 7 TABLET in 1 BOTTLE (71335-0350-1) · 71335-0350-1
- 14 TABLET in 1 BOTTLE (71335-0350-2) · 71335-0350-2
- 15 TABLET in 1 BOTTLE (71335-0350-3) · 71335-0350-3
- 28 TABLET in 1 BOTTLE (71335-0350-4) · 71335-0350-4
- 30 TABLET in 1 BOTTLE (71335-0350-5) · 71335-0350-5
- 45 TABLET in 1 BOTTLE (71335-0350-6) · 71335-0350-6
- 60 TABLET in 1 BOTTLE (71335-0350-7) · 71335-0350-7
- 42 TABLET in 1 BOTTLE (71335-0350-8) · 71335-0350-8
- 56 TABLET in 1 BOTTLE (71335-0350-9) · 71335-0350-9
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 →