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Cromolyn Sodium - 57782-397-26 - (Cromolyn Sodium)

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Drug Information of Cromolyn Sodium

Product NDC: 57782-397
Proprietary Name: Cromolyn Sodium
Non Proprietary Name: Cromolyn Sodium
Active Ingredient(s): 5.2    mg/mL & nbsp;   Cromolyn Sodium
Administration Route(s): NASAL
Dosage Form(s): SPRAY, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of Cromolyn Sodium

Product NDC: 57782-397
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075702
Marketing Category: ANDA
Start Marketing Date: 20010703

Package Information of Cromolyn Sodium

Package NDC: 57782-397-26
Package Description: 1 BOTTLE in 1 CARTON (57782-397-26) > 26 mL in 1 BOTTLE

NDC Information of Cromolyn Sodium

NDC Code 57782-397-26
Proprietary Name Cromolyn Sodium
Package Description 1 BOTTLE in 1 CARTON (57782-397-26) > 26 mL in 1 BOTTLE
Product NDC 57782-397
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cromolyn Sodium
Dosage Form Name SPRAY, METERED
Route Name NASAL
Start Marketing Date 20010703
Marketing Category Name ANDA
Labeler Name Bausch & Lomb Incorporated
Substance Name CROMOLYN SODIUM
Strength Number 5.2
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Cromolyn Sodium


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