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
- 53489-676_39e24c57-7266-2bf6-e063-6294a90afdd1
- Product NDC
- 53489-676
- Form
- TABLET
- Composition / generic term
- Phentermine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130812
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENTERMINE HYDROCHLORIDE — 37.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (53489-676-01) · 53489-676-01
- 250 TABLET in 1 BOTTLE, PLASTIC (53489-676-03) · 53489-676-03
- 500 TABLET in 1 BOTTLE, PLASTIC (53489-676-05) · 53489-676-05
- 60 TABLET in 1 BOTTLE, PLASTIC (53489-676-06) · 53489-676-06
- 30 TABLET in 1 BOTTLE, PLASTIC (53489-676-07) · 53489-676-07
- 1000 TABLET in 1 BOTTLE, PLASTIC (53489-676-10) · 53489-676-10
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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