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Cromolyn Sodium - 61314-237-10 - (Cromolyn Sodium)

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Drug Information of Cromolyn Sodium

Product NDC: 61314-237
Proprietary Name: Cromolyn Sodium
Non Proprietary Name: Cromolyn Sodium
Active Ingredient(s): 40    mg/mL & nbsp;   Cromolyn Sodium
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Cromolyn Sodium

Product NDC: 61314-237
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075282
Marketing Category: ANDA
Start Marketing Date: 19990629

Package Information of Cromolyn Sodium

Package NDC: 61314-237-10
Package Description: 10 mL in 1 BOTTLE, PLASTIC (61314-237-10)

NDC Information of Cromolyn Sodium

NDC Code 61314-237-10
Proprietary Name Cromolyn Sodium
Package Description 10 mL in 1 BOTTLE, PLASTIC (61314-237-10)
Product NDC 61314-237
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cromolyn Sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19990629
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name CROMOLYN SODIUM
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC]

Complete Information of Cromolyn Sodium


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