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"49349-160-02" National Drug Code (NDC)

Amlodipine 30 TABLET in 1 BLISTER PACK (49349-160-02)
(REMEDYREPACK INC.)

NDC Code49349-160-02
Package Description30 TABLET in 1 BLISTER PACK (49349-160-02)
Product NDC49349-160
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine
Non-Proprietary NameAmlodipine
Dosage FormTABLET
UsageORAL
Start Marketing Date20110413
Marketing Category NameANDA
Application NumberANDA076719
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/49349-160-02





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