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amlodipine besylate - 49999-248-90 - (amlodipine besylate)

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Drug Information of amlodipine besylate

Product NDC: 49999-248
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: 49999-248
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019787
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19920731

Package Information of amlodipine besylate

Package NDC: 49999-248-90
Package Description: 90 TABLET in 1 BOTTLE (49999-248-90)

NDC Information of amlodipine besylate

NDC Code 49999-248-90
Proprietary Name amlodipine besylate
Package Description 90 TABLET in 1 BOTTLE (49999-248-90)
Product NDC 49999-248
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19920731
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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