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"52125-371-19" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE (52125-371-19)
(REMEDYREPACK INC.)

NDC Code52125-371-19
Package Description90 TABLET in 1 BOTTLE (52125-371-19)
Product NDC52125-371
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20130104
Marketing Category NameANDA
Application NumberANDA077955
ManufacturerREMEDYREPACK INC.
Substance NameAMLODIPINE BESYLATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-371-19





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