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"53808-1029-1" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BLISTER PACK (53808-1029-1)
(State of Florida DOH Central Pharmacy)
NDC Code
53808-1029-1
Package Description
30 TABLET in 1 BLISTER PACK (53808-1029-1)
Product NDC
53808-1029
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20141101
Marketing Category Name
ANDA
Application Number
ANDA078414
Manufacturer
State of Florida DOH Central Pharmacy
Substance Name
AMLODIPINE BESYLATE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53808-1029-1