"68788-7679-1" National Drug Code (NDC)

Amlodipine Besylate 100 TABLET in 1 BOTTLE, PLASTIC (68788-7679-1)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7679-1
Package Description100 TABLET in 1 BOTTLE, PLASTIC (68788-7679-1)
Product NDC68788-7679
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200402
Marketing Category NameANDA
Application NumberANDA203245
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameAMLODIPINE BESYLATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

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