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Amlodipine Besylate - 55289-270-30 - (Amlodipine Besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 55289-270
Proprietary Name: Amlodipine Besylate
Non Proprietary Name: Amlodipine Besylate
Active Ingredient(s): 5    mg/1 & nbsp;   Amlodipine Besylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amlodipine Besylate

Product NDC: 55289-270
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078477
Marketing Category: ANDA
Start Marketing Date: 20100621

Package Information of Amlodipine Besylate

Package NDC: 55289-270-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-270-30)

NDC Information of Amlodipine Besylate

NDC Code 55289-270-30
Proprietary Name Amlodipine Besylate
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-270-30)
Product NDC 55289-270
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100621
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name AMLODIPINE BESYLATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Amlodipine Besylate


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