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Cromolyn Sodium - 0093-1389-43 - (cromolyn sodium)

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Drug Information of Cromolyn Sodium

Product NDC: 0093-1389
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: 0093-1389
Labeler Name: Teva Pharmaceuticals USA Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074443
Marketing Category: ANDA
Start Marketing Date: 19980526

Package Information of Cromolyn Sodium

Package NDC: 0093-1389-43
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0093-1389-43) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of Cromolyn Sodium

NDC Code 0093-1389-43
Proprietary Name Cromolyn Sodium
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0093-1389-43) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 0093-1389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cromolyn sodium
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19980526
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc.
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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