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Amlodipine Besylate - 60760-239-30 - (Amlodipine Besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 60760-239
Proprietary Name: Amlodipine Besylate
Non Proprietary Name: Amlodipine Besylate
Active Ingredient(s): 10    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: 60760-239
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077995
Marketing Category: ANDA
Start Marketing Date: 20110901

Package Information of Amlodipine Besylate

Package NDC: 60760-239-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (60760-239-30)

NDC Information of Amlodipine Besylate

NDC Code 60760-239-30
Proprietary Name Amlodipine Besylate
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (60760-239-30)
Product NDC 60760-239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine Besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110901
Marketing Category Name ANDA
Labeler Name St Marys Medical Park Pharmacy
Substance Name AMLODIPINE BESYLATE
Strength Number 10
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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