Pindolol - 0378-0052-01 - (pindolol)

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Drug Information of Pindolol

Product NDC: 0378-0052
Proprietary Name: Pindolol
Non Proprietary Name: pindolol
Active Ingredient(s): 5    mg/1 & nbsp;   pindolol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Pindolol

Product NDC: 0378-0052
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074019
Marketing Category: ANDA
Start Marketing Date: 20100722

Package Information of Pindolol

Package NDC: 0378-0052-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-0052-01)

NDC Information of Pindolol

NDC Code 0378-0052-01
Proprietary Name Pindolol
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-0052-01)
Product NDC 0378-0052
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pindolol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100722
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name PINDOLOL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Pindolol


General Information