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"53808-1100-1" National Drug Code (NDC)
Amlodipine Besylate 30 TABLET in 1 BLISTER PACK (53808-1100-1)
(DOH CENTRAL PHARMACY)
NDC Code
53808-1100-1
Package Description
30 TABLET in 1 BLISTER PACK (53808-1100-1)
Product NDC
53808-1100
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amlodipine Besylate
Non-Proprietary Name
Amlodipine Besylate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180123
Marketing Category Name
ANDA
Application Number
ANDA078552
Manufacturer
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/53808-1100-1