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amlodipine besylate - 67046-020-30 - (amlodipine besylate)

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Drug Information of amlodipine besylate

Product NDC: 67046-020
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: 67046-020
Labeler Name: Contract Pharmacy Services-PA
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: 67046-020-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-020-30)

NDC Information of amlodipine besylate

NDC Code 67046-020-30
Proprietary Name amlodipine besylate
Package Description 30 TABLET in 1 BLISTER PACK (67046-020-30)
Product NDC 67046-020
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 Contract Pharmacy Services-PA
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


General Information