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
- 71205-673_8dcaeabf-e7da-4e0c-b6db-0bd425d6506e
- Product NDC
- 71205-673
- Form
- CAPSULE
- Composition / generic term
- Benzonatate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190222
- 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 (71205-673-06) · 71205-673-06
- 10 CAPSULE in 1 BOTTLE (71205-673-10) · 71205-673-10
- 14 CAPSULE in 1 BOTTLE (71205-673-14) · 71205-673-14
- 15 CAPSULE in 1 BOTTLE (71205-673-15) · 71205-673-15
- 20 CAPSULE in 1 BOTTLE (71205-673-20) · 71205-673-20
- 21 CAPSULE in 1 BOTTLE (71205-673-21) · 71205-673-21
- 30 CAPSULE in 1 BOTTLE (71205-673-30) · 71205-673-30
- 60 CAPSULE in 1 BOTTLE (71205-673-60) · 71205-673-60
- 90 CAPSULE in 1 BOTTLE (71205-673-90) · 71205-673-90
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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