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Ipratropium Bromide - 68788-0547-2 - (Ipratropium Bromide)

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Drug Information of Ipratropium Bromide

Product NDC: 68788-0547
Proprietary Name: Ipratropium Bromide
Non Proprietary Name: Ipratropium Bromide
Active Ingredient(s): .5    mg/2.5mL & nbsp;   Ipratropium Bromide
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ipratropium Bromide

Product NDC: 68788-0547
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075562
Marketing Category: ANDA
Start Marketing Date: 20130222

Package Information of Ipratropium Bromide

Package NDC: 68788-0547-2
Package Description: 1 POUCH in 1 CARTON (68788-0547-2) > 25 VIAL, SINGLE-DOSE in 1 POUCH > 2.5 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Ipratropium Bromide

NDC Code 68788-0547-2
Proprietary Name Ipratropium Bromide
Package Description 1 POUCH in 1 CARTON (68788-0547-2) > 25 VIAL, SINGLE-DOSE in 1 POUCH > 2.5 mL in 1 VIAL, SINGLE-DOSE
Product NDC 68788-0547
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ipratropium Bromide
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20130222
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name IPRATROPIUM BROMIDE
Strength Number .5
Strength Unit mg/2.5mL
Pharmaceutical Classes Anticholinergic [EPC],Cholinergic Antagonists [MoA]

Complete Information of Ipratropium Bromide


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