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"49349-922-38" National Drug Code (NDC)

Amlodipine Besylate 3 TABLET in 1 BLISTER PACK (49349-922-38)
(REMEDYREPACK INC.)

NDC Code49349-922-38
Package Description3 TABLET in 1 BLISTER PACK (49349-922-38)
Product NDC49349-922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20130410
Marketing Category NameANDA
Application NumberANDA078925
ManufacturerREMEDYREPACK INC.
Substance NameAMLODIPINE BESYLATE
Strength5
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/49349-922-38





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