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Metipranolol - 24208-402-05 - (metipranolol)

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Drug Information of Metipranolol

Product NDC: 24208-402
Proprietary Name: Metipranolol
Non Proprietary Name: metipranolol
Active Ingredient(s): 3    mg/mL & nbsp;   metipranolol
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Metipranolol

Product NDC: 24208-402
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019907
Marketing Category: NDA
Start Marketing Date: 19891229

Package Information of Metipranolol

Package NDC: 24208-402-05
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-402-05) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Metipranolol

NDC Code 24208-402-05
Proprietary Name Metipranolol
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-402-05) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 24208-402
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metipranolol
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19891229
Marketing Category Name NDA
Labeler Name Bausch & Lomb Incorporated
Substance Name METIPRANOLOL
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metipranolol


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