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: 64850-810_f2b9f70f-b5e3-4e6e-8607-5c73afbe9677
Product NDC: 64850-810
Form: TABLET
Composition / generic term: Phentermine Hydrochloride
Labeler: Elite Laboratories, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20140501
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 (64850-810-01) · 64850-810-01
1000 TABLET in 1 BOTTLE (64850-810-10) · 64850-810-10

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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