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
65841-843_fb123061-e971-4394-aa10-ae733de31be1
Product NDC
65841-843
Form
CAPSULE
Composition / generic term
Benzonatate
Labeler
Zydus Lifesciences Limited
Marketing category
ANDA
Marketing start / end (source format)
20070904
Source listing expiry
20261231

Source-listed ingredients

  • BENZONATATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (65841-843-01) · 65841-843-01

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.

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Benzonatate — United States | Molindra Medicines