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Cyclopentolate Hydrochloride - 24208-735-01 - (Cyclopentolate Hydrochloride)

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Drug Information of Cyclopentolate Hydrochloride

Product NDC: 24208-735
Proprietary Name: Cyclopentolate Hydrochloride
Non Proprietary Name: Cyclopentolate Hydrochloride
Active Ingredient(s): 10    mg/mL & nbsp;   Cyclopentolate Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclopentolate Hydrochloride

Product NDC: 24208-735
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040075
Marketing Category: ANDA
Start Marketing Date: 19940429

Package Information of Cyclopentolate Hydrochloride

Package NDC: 24208-735-01
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-735-01) > 2 mL in 1 BOTTLE, DROPPER

NDC Information of Cyclopentolate Hydrochloride

NDC Code 24208-735-01
Proprietary Name Cyclopentolate Hydrochloride
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-735-01) > 2 mL in 1 BOTTLE, DROPPER
Product NDC 24208-735
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclopentolate Hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19940429
Marketing Category Name ANDA
Labeler Name Bausch & Lomb Incorporated
Substance Name CYCLOPENTOLATE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Cyclopentolate Hydrochloride


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