NDC 71335-3169 – Benzonatate

Benzonatate 200 mg/1 · Capsule, Liquid Filled · Oral

Human Prescription Drug

Product NDC71335-3169

Product details

Brand name
Benzonatate
Generic name
Benzonatate
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Liquid Filled
Route
Oral
Marketing category
ANDA · ANDA040682
Marketed since
September 29, 2024
Listing expires
December 31, 2027
Pharmacologic class
Non-narcotic Antitussive

Active ingredients

Uses, dosage, side effects and warnings for Benzonatate →

Package NDC codes (4)

Package NDCDescriptionSince
71335-3169-121 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-1)Aug 11, 2026
71335-3169-2100 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-2)Aug 11, 2026
71335-3169-3500 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-3)Aug 11, 2026
71335-3169-410 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3169-4)Aug 11, 2026

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