Betoptic S - 0065-0246-15 - (betaxolol hydrochloride)

Alphabetical Index


Drug Information of Betoptic S

Product NDC: 0065-0246
Proprietary Name: Betoptic S
Non Proprietary Name: betaxolol hydrochloride
Active Ingredient(s): 2.8    mg/mL & nbsp;   betaxolol hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Betoptic S

Product NDC: 0065-0246
Labeler Name: Alcon Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019845
Marketing Category: NDA
Start Marketing Date: 19960115

Package Information of Betoptic S

Package NDC: 0065-0246-15
Package Description: 15 mL in 1 BOTTLE, PLASTIC (0065-0246-15)

NDC Information of Betoptic S

NDC Code 0065-0246-15
Proprietary Name Betoptic S
Package Description 15 mL in 1 BOTTLE, PLASTIC (0065-0246-15)
Product NDC 0065-0246
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name betaxolol hydrochloride
Dosage Form Name SUSPENSION
Route Name OPHTHALMIC
Start Marketing Date 19960115
Marketing Category Name NDA
Labeler Name Alcon Laboratories, Inc.
Substance Name BETAXOLOL HYDROCHLORIDE
Strength Number 2.8
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Betoptic S


General Information