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
- 71335-1840_629f541a-8b78-48b2-bb97-1b072195dd83
- Product NDC
- 71335-1840
- Form
- TABLET
- Composition / generic term
- PHENDIMETRAZINE TARTRATE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180701
- 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 (71335-1840-0) · 71335-1840-0
- 30 TABLET in 1 BOTTLE (71335-1840-1) · 71335-1840-1
- 90 TABLET in 1 BOTTLE (71335-1840-2) · 71335-1840-2
- 15 TABLET in 1 BOTTLE (71335-1840-3) · 71335-1840-3
- 60 TABLET in 1 BOTTLE (71335-1840-4) · 71335-1840-4
- 7 TABLET in 1 BOTTLE (71335-1840-5) · 71335-1840-5
- 21 TABLET in 1 BOTTLE (71335-1840-6) · 71335-1840-6
- 42 TABLET in 1 BOTTLE (71335-1840-7) · 71335-1840-7
- 100 TABLET in 1 BOTTLE (71335-1840-8) · 71335-1840-8
- 28 TABLET in 1 BOTTLE (71335-1840-9) · 71335-1840-9
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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