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
- 70518-2873_57d4abd7-5638-daab-e063-6394a90a029f
- Product NDC
- 70518-2873
- Form
- CAPSULE
- Composition / generic term
- Benzonatate
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200909
- Source listing expiry
- 20271231
Source-listed ingredients
- BENZONATATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 CAPSULE in 1 BOTTLE, PLASTIC (70518-2873-0) · 70518-2873-0
- 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-2873-2) · 70518-2873-2
- 15 CAPSULE in 1 BOTTLE, PLASTIC (70518-2873-7) · 70518-2873-7
- 50 POUCH in 1 BOX (70518-2873-8) / 1 CAPSULE in 1 POUCH (70518-2873-9) · 70518-2873-8
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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