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
- 63187-800_4e1cdc95-3d6c-4a43-8aec-194daf2abd12
- Product NDC
- 63187-800
- Form
- TABLET
- Composition / generic term
- Phentermine Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110610
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENTERMINE HYDROCHLORIDE — 37.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 TABLET in 1 BOTTLE (63187-800-07) · 63187-800-07
- 14 TABLET in 1 BOTTLE (63187-800-14) · 63187-800-14
- 15 TABLET in 1 BOTTLE (63187-800-15) · 63187-800-15
- 30 TABLET in 1 BOTTLE (63187-800-30) · 63187-800-30
- 60 TABLET in 1 BOTTLE (63187-800-60) · 63187-800-60
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 →