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
63187-076_1e43585a-8e75-4a75-a011-56b5f80cb7cd
Product NDC
63187-076
Form
CAPSULE, LIQUID FILLED
Composition / generic term
Benzonatate
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20100604
Source listing expiry
20261231

Source-listed ingredients

  • BENZONATATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 14 CAPSULE, LIQUID FILLED in 1 BOTTLE (63187-076-14) · 63187-076-14
  • 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (63187-076-20) · 63187-076-20
  • 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (63187-076-30) · 63187-076-30
  • 40 CAPSULE, LIQUID FILLED in 1 BOTTLE (63187-076-40) · 63187-076-40

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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