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
- 71205-605_2fae3438-3fe9-4f4f-bd89-35fb7050c560
- Product NDC
- 71205-605
- Form
- CAPSULE
- Composition / generic term
- Benzonatate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160815
- Source listing expiry
- 20261231
Source-listed ingredients
- BENZONATATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-10) · 71205-605-10
- 14 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-14) · 71205-605-14
- 15 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-15) · 71205-605-15
- 20 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-20) · 71205-605-20
- 21 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-21) · 71205-605-21
- 30 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-30) · 71205-605-30
- 40 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-40) · 71205-605-40
- 60 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-60) · 71205-605-60
- 90 CAPSULE in 1 BOTTLE, PLASTIC (71205-605-90) · 71205-605-90
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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