United States · FDA National Drug Code directory
Benzonatate
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
- 71335-2590_7ed224eb-c573-4dea-a156-3f9b4e536a0f
- Product NDC
- 71335-2590
- Form
- CAPSULE
- Composition / generic term
- Benzonatate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070409
- Source listing expiry
- 20261231
Source-listed ingredients
- BENZONATATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 CAPSULE in 1 BOTTLE (71335-2590-0) · 71335-2590-0
- 30 CAPSULE in 1 BOTTLE (71335-2590-1) · 71335-2590-1
- 100 CAPSULE in 1 BOTTLE (71335-2590-2) · 71335-2590-2
- 45 CAPSULE in 1 BOTTLE (71335-2590-3) · 71335-2590-3
- 20 CAPSULE in 1 BOTTLE (71335-2590-4) · 71335-2590-4
- 15 CAPSULE in 1 BOTTLE (71335-2590-5) · 71335-2590-5
- 21 CAPSULE in 1 BOTTLE (71335-2590-6) · 71335-2590-6
- 60 CAPSULE in 1 BOTTLE (71335-2590-7) · 71335-2590-7
- 50 CAPSULE in 1 BOTTLE (71335-2590-8) · 71335-2590-8
- 90 CAPSULE in 1 BOTTLE (71335-2590-9) · 71335-2590-9
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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