NDC 71335-1329 – Benzonatate

Benzonatate 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1329

Product details

Brand name
Benzonatate
Generic name
Benzonatate
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA040627
Marketed since
March 22, 2017
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
71335-1329-010 CAPSULE in 1 BOTTLE (71335-1329-0)Mar 22, 2017
71335-1329-130 CAPSULE in 1 BOTTLE (71335-1329-1)Mar 22, 2017
71335-1329-220 CAPSULE in 1 BOTTLE (71335-1329-2)Mar 22, 2017
71335-1329-3100 CAPSULE in 1 BOTTLE (71335-1329-3)Mar 22, 2017
71335-1329-415 CAPSULE in 1 BOTTLE (71335-1329-4)Mar 22, 2017
71335-1329-5120 CAPSULE in 1 BOTTLE (71335-1329-5)Mar 22, 2017
71335-1329-660 CAPSULE in 1 BOTTLE (71335-1329-6)Mar 22, 2017
71335-1329-790 CAPSULE in 1 BOTTLE (71335-1329-7)Mar 22, 2017
71335-1329-814 CAPSULE in 1 BOTTLE (71335-1329-8)Mar 22, 2017
71335-1329-940 CAPSULE in 1 BOTTLE (71335-1329-9)Mar 22, 2017

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