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Ipratropium Bromide and Albuterol Sulfate - 0591-3433-30 - (Ipratropium Bromide and Albuterol Sulfate)

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Drug Information of Ipratropium Bromide and Albuterol Sulfate

Product NDC: 0591-3433
Proprietary Name: Ipratropium Bromide and Albuterol Sulfate
Non Proprietary Name: Ipratropium Bromide and Albuterol Sulfate
Active Ingredient(s): 2.5; .5    mg/3mL; mg/3mL & nbsp;   Ipratropium Bromide and Albuterol Sulfate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ipratropium Bromide and Albuterol Sulfate

Product NDC: 0591-3433
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077559
Marketing Category: ANDA
Start Marketing Date: 20071231

Package Information of Ipratropium Bromide and Albuterol Sulfate

Package NDC: 0591-3433-30
Package Description: 6 POUCH in 1 CARTON (0591-3433-30) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL

NDC Information of Ipratropium Bromide and Albuterol Sulfate

NDC Code 0591-3433-30
Proprietary Name Ipratropium Bromide and Albuterol Sulfate
Package Description 6 POUCH in 1 CARTON (0591-3433-30) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL
Product NDC 0591-3433
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ipratropium Bromide and Albuterol Sulfate
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20071231
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name ALBUTEROL SULFATE; IPRATROPIUM BROMIDE
Strength Number 2.5; .5
Strength Unit mg/3mL; mg/3mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Ipratropium Bromide and Albuterol Sulfate


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