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
- 71335-3169_538a5bfe-55bc-4a5c-8259-f40c4c394d63
- Product NDC
- 71335-3169
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Benzonatate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240929
- Source listing expiry
- 20271231
Source-listed ingredients
- BENZONATATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-1) · 71335-3169-1
- 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-2) · 71335-3169-2
- 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-3) · 71335-3169-3
- 10 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-4) · 71335-3169-4
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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