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Ipratropium Bromide and Albuterol Sulfate - 0378-9671-93 - (Ipratropium Bromide and Albuterol Sulfate)

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Drug Information of Ipratropium Bromide and Albuterol Sulfate

Product NDC: 0378-9671
Proprietary Name: Ipratropium Bromide and Albuterol Sulfate
Non Proprietary Name: Ipratropium Bromide and Albuterol Sulfate
Active Ingredient(s): 3; .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: 0378-9671
Labeler Name: Mylan Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202496
Marketing Category: ANDA
Start Marketing Date: 20130301

Package Information of Ipratropium Bromide and Albuterol Sulfate

Package NDC: 0378-9671-93
Package Description: 30 POUCH in 1 CARTON (0378-9671-93) > 1 AMPULE in 1 POUCH (0378-9671-31) > 3 mL in 1 AMPULE

NDC Information of Ipratropium Bromide and Albuterol Sulfate

NDC Code 0378-9671-93
Proprietary Name Ipratropium Bromide and Albuterol Sulfate
Package Description 30 POUCH in 1 CARTON (0378-9671-93) > 1 AMPULE in 1 POUCH (0378-9671-31) > 3 mL in 1 AMPULE
Product NDC 0378-9671
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 20130301
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals, Inc.
Substance Name ALBUTEROL SULFATE; IPRATROPIUM BROMIDE
Strength Number 3; .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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