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NDC 68180-0281-13 Ethambutol Hydrochloride 400 mg/1 Details

Ethambutol Hydrochloride 400 mg/1

Ethambutol Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. 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: 68180-0281-13
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Ethambutol

Product Information

NDC	68180-0281
Product ID	68180-281_dbe51867-ce72-4fbe-92d7-e5e95190339f
Associated GPIs	09000040100310
GCN Sequence Number	009426
GCN Sequence Number Description	ethambutol HCl TABLET 400 MG ORAL
HIC3	W2E
HIC3 Description	ANTI-MYCOBACTERIUM AGENTS
GCN	41801
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
Route	ORAL
Active Ingredient Strength	400
Active Ingredient Units	mg/1
Substance Name	ETHAMBUTOL HYDROCHLORIDE
Labeler Name	Lupin Pharmaceuticals, Inc.
Pharmaceutical Class	Antimycobacterial [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078939
Listing Certified Through	2024-12-31

Package

NDC 68180-0281-13 (68180028113)

Pricing Information	N/A
NDC Package Code	68180-281-13
Billing NDC	68180028113
Package	4 BLISTER PACK in 1 CARTON (68180-281-13) / 14 TABLET in 1 BLISTER PACK (68180-281-11)
Marketing Start Date	2009-07-04
NDC Exclude Flag	N