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
- 50090-5409_5332f31c-1d81-49d0-9f5f-71c99d88896c
- Product NDC
- 50090-5409
- Form
- CAPSULE
- Composition / generic term
- Benzonatate
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181221
- Source listing expiry
- 20271231
Source-listed ingredients
- BENZONATATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 CAPSULE in 1 BOTTLE (50090-5409-0) · 50090-5409-0
- 24 CAPSULE in 1 BOTTLE (50090-5409-1) · 50090-5409-1
- 30 CAPSULE in 1 BOTTLE (50090-5409-2) · 50090-5409-2
- 15 CAPSULE in 1 BOTTLE (50090-5409-5) · 50090-5409-5
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →