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"69367-265-01" National Drug Code (NDC)
Felodipine 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-265-01)
(Westminster Pharmaceuticals, LLC)
NDC Code
69367-265-01
Package Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-265-01)
Product NDC
69367-265
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Felodipine
Non-Proprietary Name
Felodipine
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20230331
Marketing Category Name
ANDA
Application Number
ANDA210847
Manufacturer
Westminster Pharmaceuticals, LLC
Substance Name
FELODIPINE
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/69367-265-01