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Amlodipine Besylate - 49349-922-38 - (Amlodipine besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 49349-922
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: 49349-922
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078925
Marketing Category: ANDA
Start Marketing Date: 20130410

Package Information of Amlodipine Besylate

Package NDC: 49349-922-38
Package Description: 3 TABLET in 1 BLISTER PACK (49349-922-38)

NDC Information of Amlodipine Besylate

NDC Code 49349-922-38
Proprietary Name Amlodipine Besylate
Package Description 3 TABLET in 1 BLISTER PACK (49349-922-38)
Product NDC 49349-922
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amlodipine besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130410
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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