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NDC 71335-0031-01 Benzonatate 200 mg/1 Details

Benzonatate 200 mg/1

Benzonatate is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is BENZONATATE.

MedlinePlus Drug Summary

Benzonatate is used to relieve cough. Benzonatate is in a class of medications called antitussives (cough suppressants). It works by reducing the cough reflex in the lungs and air passages.

Related Packages: 71335-0031-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Benzonatate

Product Information

NDC	71335-0031
Product ID	71335-0031_8047b865-7441-4e23-b1d1-7d48a77b8703
Associated GPIs	43102010000110
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Benzonatate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Benzonatate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	CAPSULE
Route	ORAL
Active Ingredient Strength	200
Active Ingredient Units	mg/1
Substance Name	BENZONATATE
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	Decreased Tracheobronchial Stretch Receptor Activity [PE], Non-narcotic Antitussive [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA202765
Listing Certified Through	2024-12-31

Package

NDC 71335-0031-01 (71335003101)

Pricing Information	N/A
NDC Package Code	71335-0031-1
Billing NDC	71335003101
Package	30 CAPSULE in 1 BOTTLE (71335-0031-1)
Marketing Start Date	2018-02-27
NDC Exclude Flag	N