"52125-642-02" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BLISTER PACK (52125-642-02)
(REMEDYREPACK INC.)

NDC Code52125-642-02
Package Description30 TABLET in 1 BLISTER PACK (52125-642-02)
Product NDC52125-642
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20130614
Marketing Category NameANDA
Application NumberANDA078925
ManufacturerREMEDYREPACK INC.
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

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