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Cyclopentolate Hydrochloride - 61314-397-01 - (Cyclopentolate Hydrochloride)

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Drug Information of Cyclopentolate Hydrochloride

Product NDC: 61314-397
Proprietary Name: Cyclopentolate Hydrochloride
Non Proprietary Name: Cyclopentolate Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Cyclopentolate Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclopentolate Hydrochloride

Product NDC: 61314-397
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084108
Marketing Category: ANDA
Start Marketing Date: 20020822

Package Information of Cyclopentolate Hydrochloride

Package NDC: 61314-397-01
Package Description: 2 mL in 1 BOTTLE (61314-397-01)

NDC Information of Cyclopentolate Hydrochloride

NDC Code 61314-397-01
Proprietary Name Cyclopentolate Hydrochloride
Package Description 2 mL in 1 BOTTLE (61314-397-01)
Product NDC 61314-397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclopentolate Hydrochloride
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20020822
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name CYCLOPENTOLATE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Cyclopentolate Hydrochloride


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