United States · FDA National Drug Code directory
Benzonatate 100 mg
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
- 25000-002_8668f10d-45dc-4248-88ac-6e8c5d576435
- Product NDC
- 25000-002
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Benzonatate 100 mg
- Labeler
- MARKSANS PHARMA LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260410
- Source listing expiry
- 20271231
Source-listed ingredients
- BENZONATATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (25000-002-03) · 25000-002-03
- 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (25000-002-08) · 25000-002-08
- 500 CAPSULE, LIQUID FILLED in 1 BOTTLE (25000-002-12) · 25000-002-12
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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