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
- 10702-067_7d787b5e-b8c6-1ca4-e053-2991aa0a464b
- Product NDC
- 10702-067
- Form
- TABLET
- Composition / generic term
- Phentermine Hydrochloride
- Labeler
- KVK-TECH, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180329
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENTERMINE HYDROCHLORIDE — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (10702-067-03) · 10702-067-03
- 5000 TABLET in 1 BOTTLE (10702-067-05) · 10702-067-05
- 1000 TABLET in 1 BOTTLE (10702-067-10) · 10702-067-10
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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