United States · FDA National Drug Code directory
Phendimetrazine Tartrate
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
- 71335-0074_e2bbffcf-c0cc-4dbc-b5e4-cdc5fd7cd0c2
- Product NDC
- 71335-0074
- Form
- TABLET
- Composition / generic term
- Phendimetrazine Tartrate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100915
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENDIMETRAZINE TARTRATE — 35 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (71335-0074-0) · 71335-0074-0
- 30 TABLET in 1 BOTTLE (71335-0074-1) · 71335-0074-1
- 135 TABLET in 1 BOTTLE (71335-0074-2) · 71335-0074-2
- 180 TABLET in 1 BOTTLE (71335-0074-3) · 71335-0074-3
- 15 TABLET in 1 BOTTLE (71335-0074-4) · 71335-0074-4
- 90 TABLET in 1 BOTTLE (71335-0074-5) · 71335-0074-5
- 7 TABLET in 1 BOTTLE (71335-0074-6) · 71335-0074-6
- 21 TABLET in 1 BOTTLE (71335-0074-7) · 71335-0074-7
- 60 TABLET in 1 BOTTLE (71335-0074-8) · 71335-0074-8
- 45 TABLET in 1 BOTTLE (71335-0074-9) · 71335-0074-9
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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