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: 68382-091_00b5fd87-d6cb-4a95-b835-4e9c1232768b
Product NDC: 68382-091
Form: CAPSULE, LIQUID FILLED
Composition / generic term: Benzonatate
Labeler: Zydus Pharmaceuticals USA Inc.
Marketing category: ANDA
Marketing start / end (source format): 20070409
Source listing expiry: 20271231

Source-listed ingredients

BENZONATATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 CAPSULE, LIQUID FILLED in 1 BOTTLE (68382-091-01) · 68382-091-01

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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