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NDC 54879-0001-01 Ethambutol Hydrochloride 100 mg/1 Details

Ethambutol Hydrochloride 100 mg/1

Ethambutol Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by STI Pharma LLC. The primary component is ETHAMBUTOL HYDROCHLORIDE.

MedlinePlus Drug Summary

Ethambutol eliminates certain bacteria that cause tuberculosis (TB). It is used with other medicines to treat tuberculosis and to prevent you from giving the infection to others. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 54879-0001-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Ethambutol

Product Information

NDC	54879-0001
Product ID	54879-001_0ec564dd-5593-52ee-e063-6294a90a34de
Associated GPIs	09000040100305
GCN Sequence Number	009425
GCN Sequence Number Description	ethambutol HCl TABLET 100 MG ORAL
HIC3	W2E
HIC3 Description	ANTI-MYCOBACTERIUM AGENTS
GCN	41800
HICL Sequence Number	004085
HICL Sequence Number Description	ETHAMBUTOL HCL
Brand/Generic	Generic
Proprietary Name	Ethambutol Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Ethambutol Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	ETHAMBUTOL HYDROCHLORIDE
Labeler Name	STI Pharma LLC
Pharmaceutical Class	Antimycobacterial [EPC]
DEA Schedule	n/a
Marketing Category	NDA AUTHORIZED GENERIC
Application Number	NDA016320
Listing Certified Through	2025-12-31

Package

NDC 54879-0001-01 (54879000101)

Pricing Information	N/A
NDC Package Code	54879-001-01
Billing NDC	54879000101
Package	12 CARTON in 1 BOX (54879-001-01) / 12 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date	2006-12-15
NDC Exclude Flag	N