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Nedocromil Sodium - 17478-066-10 - (Nedocromil Sodium)

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Drug Information of Nedocromil Sodium

Product NDC: 17478-066
Proprietary Name: Nedocromil Sodium
Non Proprietary Name: Nedocromil Sodium
Active Ingredient(s): 20    mg/mL & nbsp;   Nedocromil Sodium
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Nedocromil Sodium

Product NDC: 17478-066
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090638
Marketing Category: ANDA
Start Marketing Date: 20120910

Package Information of Nedocromil Sodium

Package NDC: 17478-066-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (17478-066-10) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Nedocromil Sodium

NDC Code 17478-066-10
Proprietary Name Nedocromil Sodium
Package Description 1 BOTTLE, DROPPER in 1 CARTON (17478-066-10) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 17478-066
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nedocromil Sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20120910
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name NEDOCROMIL SODIUM
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC]

Complete Information of Nedocromil Sodium


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