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"48792-7841-1" National Drug Code (NDC)

Amlodipine Besylate 90 TABLET in 1 BOTTLE, PLASTIC (48792-7841-1)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7841-1
Package Description90 TABLET in 1 BOTTLE, PLASTIC (48792-7841-1)
Product NDC48792-7841
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180507
Marketing Category NameANDA
Application NumberANDA206524
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/48792-7841-1





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