NDC 71335-0031 – Benzonatate

Benzonatate 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0031

Product details

Brand name
Benzonatate
Generic name
Benzonatate
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202765
Marketed since
August 10, 2015
Listing expires
December 31, 2026
Pharmacologic class
Non-narcotic Antitussive

Active ingredients

Uses, dosage, side effects and warnings for Benzonatate →

Package NDC codes (9)

Package NDCDescriptionSince
71335-0031-130 CAPSULE in 1 BOTTLE (71335-0031-1)Feb 27, 2018
71335-0031-2100 CAPSULE in 1 BOTTLE (71335-0031-2)Sep 28, 2022
71335-0031-345 CAPSULE in 1 BOTTLE (71335-0031-3)Sep 28, 2022
71335-0031-420 CAPSULE in 1 BOTTLE (71335-0031-4)Dec 15, 2021
71335-0031-515 CAPSULE in 1 BOTTLE (71335-0031-5)Feb 19, 2018
71335-0031-621 CAPSULE in 1 BOTTLE (71335-0031-6)Mar 2, 2018
71335-0031-760 CAPSULE in 1 BOTTLE (71335-0031-7)Sep 28, 2022
71335-0031-850 CAPSULE in 1 BOTTLE (71335-0031-8)Sep 28, 2022
71335-0031-990 CAPSULE in 1 BOTTLE (71335-0031-9)Sep 28, 2022

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