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
71335-2021_e1c77f1a-79d0-4c5d-a011-fd5c8cd59ffe
Product NDC
71335-2021
Form
CAPSULE
Composition / generic term
BENZONATATE
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20180501
Source listing expiry
20261231

Source-listed ingredients

  • BENZONATATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 CAPSULE in 1 BOTTLE (71335-2021-1) · 71335-2021-1
  • 100 CAPSULE in 1 BOTTLE (71335-2021-2) · 71335-2021-2
  • 45 CAPSULE in 1 BOTTLE (71335-2021-3) · 71335-2021-3
  • 20 CAPSULE in 1 BOTTLE (71335-2021-4) · 71335-2021-4
  • 15 CAPSULE in 1 BOTTLE (71335-2021-5) · 71335-2021-5
  • 21 CAPSULE in 1 BOTTLE (71335-2021-6) · 71335-2021-6
  • 60 CAPSULE in 1 BOTTLE (71335-2021-7) · 71335-2021-7
  • 50 CAPSULE in 1 BOTTLE (71335-2021-8) · 71335-2021-8
  • 90 CAPSULE in 1 BOTTLE (71335-2021-9) · 71335-2021-9

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.

Browse United States records →