NDC 71335-2590 – Benzonatate

Benzonatate 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2590

Product details

Brand name
Benzonatate
Generic name
Benzonatate
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA040597
Marketed since
April 9, 2007
Listing expires
December 31, 2026
Pharmacologic class
Non-narcotic Antitussive

Active ingredients

Uses, dosage, side effects and warnings for Benzonatate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2590-06 CAPSULE in 1 BOTTLE (71335-2590-0)Jun 4, 2025
71335-2590-130 CAPSULE in 1 BOTTLE (71335-2590-1)Jun 4, 2025
71335-2590-2100 CAPSULE in 1 BOTTLE (71335-2590-2)Jun 4, 2025
71335-2590-345 CAPSULE in 1 BOTTLE (71335-2590-3)Jun 4, 2025
71335-2590-420 CAPSULE in 1 BOTTLE (71335-2590-4)Jun 4, 2025
71335-2590-515 CAPSULE in 1 BOTTLE (71335-2590-5)Jun 4, 2025
71335-2590-621 CAPSULE in 1 BOTTLE (71335-2590-6)Jun 4, 2025
71335-2590-760 CAPSULE in 1 BOTTLE (71335-2590-7)Jun 4, 2025
71335-2590-850 CAPSULE in 1 BOTTLE (71335-2590-8)Jun 4, 2025
71335-2590-990 CAPSULE in 1 BOTTLE (71335-2590-9)Jun 4, 2025

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