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NDC 62135-0672-90 Albuterol Sulfate 4 mg/1 Details

Albuterol Sulfate 4 mg/1

Albuterol Sulfate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is ALBUTEROL SULFATE.

MedlinePlus Drug Summary

Albuterol is used to prevent and treat wheezing, difficulty breathing, chest tightness, and coughing caused by lung diseases such as asthma and chronic obstructive pulmonary disease (COPD; a group of diseases that affect the lungs and airways). Albuterol is in a class of medications called bronchodilators. It works by relaxing and opening the air passages to the lungs to make breathing easier.

Related Packages: 62135-0672-90
Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Albuterol

Product Information

NDC	62135-0672
Product ID	62135-672_fe7cbf82-9f32-327e-e053-6294a90aebc8
Associated GPIs
GCN Sequence Number	005034
GCN Sequence Number Description	albuterol sulfate TABLET 4 MG ORAL
HIC3	J5D
HIC3 Description	BETA-ADRENERGIC AGENTS
GCN	20101
HICL Sequence Number	002073
HICL Sequence Number Description	ALBUTEROL SULFATE
Brand/Generic	Generic
Proprietary Name	Albuterol Sulfate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Albuterol Sulfate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	4
Active Ingredient Units	mg/1
Substance Name	ALBUTEROL SULFATE
Labeler Name	Chartwell RX, LLC
Pharmaceutical Class	Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA072151
Listing Certified Through	2024-12-31

Package

NDC 62135-0672-90 (62135067290)

Pricing Information	N/A
NDC Package Code	62135-672-90
Billing NDC	62135067290
Package	90 TABLET in 1 BOTTLE (62135-672-90)
Marketing Start Date	2023-06-14
NDC Exclude Flag	N