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Cyclomydril - 0065-0359-02 - (cyclopentolate hydrochloride and phenylephrine hydrochloride)

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Drug Information of Cyclomydril

Product NDC: 0065-0359
Proprietary Name: Cyclomydril
Non Proprietary Name: cyclopentolate hydrochloride and phenylephrine hydrochloride
Active Ingredient(s): 2; 10    mg/mL; mg/mL & nbsp;   cyclopentolate hydrochloride and phenylephrine hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclomydril

Product NDC: 0065-0359
Labeler Name: Alcon Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084300
Marketing Category: ANDA
Start Marketing Date: 19580630

Package Information of Cyclomydril

Package NDC: 0065-0359-02
Package Description: 2 mL in 1 BOTTLE, PLASTIC (0065-0359-02)

NDC Information of Cyclomydril

NDC Code 0065-0359-02
Proprietary Name Cyclomydril
Package Description 2 mL in 1 BOTTLE, PLASTIC (0065-0359-02)
Product NDC 0065-0359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cyclopentolate hydrochloride and phenylephrine hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19580630
Marketing Category Name ANDA
Labeler Name Alcon Laboratories, Inc.
Substance Name CYCLOPENTOLATE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 2; 10
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Cyclomydril


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