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
- 71205-972_492a0004-9824-4df9-ab03-a46953aa4fdb
- Product NDC
- 71205-972
- Form
- CAPSULE
- Composition / generic term
- benzonatate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170322
- Source listing expiry
- 20261231
Source-listed ingredients
- BENZONATATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (71205-972-00) · 71205-972-00
- 10 CAPSULE in 1 BOTTLE (71205-972-10) · 71205-972-10
- 14 CAPSULE in 1 BOTTLE (71205-972-14) · 71205-972-14
- 15 CAPSULE in 1 BOTTLE (71205-972-15) · 71205-972-15
- 20 CAPSULE in 1 BOTTLE (71205-972-20) · 71205-972-20
- 21 CAPSULE in 1 BOTTLE (71205-972-21) · 71205-972-21
- 30 CAPSULE in 1 BOTTLE (71205-972-30) · 71205-972-30
- 500 CAPSULE in 1 BOTTLE (71205-972-55) · 71205-972-55
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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