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
- 71335-0031_8047b865-7441-4e23-b1d1-7d48a77b8703
- Product NDC
- 71335-0031
- Form
- CAPSULE
- Composition / generic term
- Benzonatate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150810
- Source listing expiry
- 20261231
Source-listed ingredients
- BENZONATATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (71335-0031-1) · 71335-0031-1
- 100 CAPSULE in 1 BOTTLE (71335-0031-2) · 71335-0031-2
- 45 CAPSULE in 1 BOTTLE (71335-0031-3) · 71335-0031-3
- 20 CAPSULE in 1 BOTTLE (71335-0031-4) · 71335-0031-4
- 15 CAPSULE in 1 BOTTLE (71335-0031-5) · 71335-0031-5
- 21 CAPSULE in 1 BOTTLE (71335-0031-6) · 71335-0031-6
- 60 CAPSULE in 1 BOTTLE (71335-0031-7) · 71335-0031-7
- 50 CAPSULE in 1 BOTTLE (71335-0031-8) · 71335-0031-8
- 90 CAPSULE in 1 BOTTLE (71335-0031-9) · 71335-0031-9
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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