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Carteolol Hydrochloride - 61314-238-05 - (Carteolol Hydrochloride)

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Drug Information of Carteolol Hydrochloride

Product NDC: 61314-238
Proprietary Name: Carteolol Hydrochloride
Non Proprietary Name: Carteolol Hydrochloride
Active Ingredient(s): 10    mg/mL & nbsp;   Carteolol Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Carteolol Hydrochloride

Product NDC: 61314-238
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075476
Marketing Category: ANDA
Start Marketing Date: 20000105

Package Information of Carteolol Hydrochloride

Package NDC: 61314-238-05
Package Description: 5 mL in 1 BOTTLE, PLASTIC (61314-238-05)

NDC Information of Carteolol Hydrochloride

NDC Code 61314-238-05
Proprietary Name Carteolol Hydrochloride
Package Description 5 mL in 1 BOTTLE, PLASTIC (61314-238-05)
Product NDC 61314-238
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carteolol Hydrochloride
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20000105
Marketing Category Name ANDA
Labeler Name Sandoz Inc.
Substance Name CARTEOLOL HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Carteolol Hydrochloride


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