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Ipratropium Bromide - 0487-9801-02 - (Ipratropium Bromide)

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Drug Information of Ipratropium Bromide

Product NDC: 0487-9801
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: 0487-9801
Labeler Name: Nephron Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075562
Marketing Category: ANDA
Start Marketing Date: 20010927

Package Information of Ipratropium Bromide

Package NDC: 0487-9801-02
Package Description: 30 BAG in 1 BOX (0487-9801-02) > 1 POUCH in 1 BAG > 1 VIAL, SINGLE-DOSE in 1 POUCH > 2.5 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Ipratropium Bromide

NDC Code 0487-9801-02
Proprietary Name Ipratropium Bromide
Package Description 30 BAG in 1 BOX (0487-9801-02) > 1 POUCH in 1 BAG > 1 VIAL, SINGLE-DOSE in 1 POUCH > 2.5 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0487-9801
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ipratropium Bromide
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20010927
Marketing Category Name ANDA
Labeler Name Nephron Pharmaceuticals Corporation
Substance Name IPRATROPIUM BROMIDE
Strength Number .5
Strength Unit mg/2.5mL
Pharmaceutical Classes

Complete Information of Ipratropium Bromide


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