"68788-8313-3" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BOTTLE, PLASTIC (68788-8313-3)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-8313-3
Package Description30 TABLET in 1 BOTTLE, PLASTIC (68788-8313-3)
Product NDC68788-8313
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20221221
Marketing Category NameANDA
Application NumberANDA203245
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameAMLODIPINE BESYLATE
Strength5
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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