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Ipratropium Bromide and Albuterol Sulfate - 0378-6988-93 - (ipratropium bromide and albuterol sulfate)

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Drug Information of Ipratropium Bromide and Albuterol Sulfate

Product NDC: 0378-6988
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: 0378-6988
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020950
Marketing Category: NDA
Start Marketing Date: 20010321

Package Information of Ipratropium Bromide and Albuterol Sulfate

Package NDC: 0378-6988-93
Package Description: 30 POUCH in 1 CARTON (0378-6988-93) > 1 VIAL in 1 POUCH > 3 mL in 1 VIAL

NDC Information of Ipratropium Bromide and Albuterol Sulfate

NDC Code 0378-6988-93
Proprietary Name Ipratropium Bromide and Albuterol Sulfate
Package Description 30 POUCH in 1 CARTON (0378-6988-93) > 1 VIAL in 1 POUCH > 3 mL in 1 VIAL
Product NDC 0378-6988
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 20010321
Marketing Category Name NDA
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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