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Metipranolol - 61314-447-10 - (Metipranolol)

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Drug Information of Metipranolol

Product NDC: 61314-447
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: 61314-447
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075720
Marketing Category: ANDA
Start Marketing Date: 20010809

Package Information of Metipranolol

Package NDC: 61314-447-10
Package Description: 10 mL in 1 BOTTLE, PLASTIC (61314-447-10)

NDC Information of Metipranolol

NDC Code 61314-447-10
Proprietary Name Metipranolol
Package Description 10 mL in 1 BOTTLE, PLASTIC (61314-447-10)
Product NDC 61314-447
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metipranolol
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20010809
Marketing Category Name ANDA
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name METIPRANOLOL
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metipranolol


General Information