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"24555-0199-3" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BLISTER PACK (24555-0199-3)
(Correct Rx Pharmacy Services, Inc.)
NDC Code
24555-0199-3
Package Description
30 TABLET in 1 BLISTER PACK (24555-0199-3)
Product NDC
24555-0199
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20240101
Marketing Category Name
ANDA
Application Number
ANDA078925
Manufacturer
Correct Rx Pharmacy Services, Inc.
Substance Name
AMLODIPINE BESYLATE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/24555-0199-3