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"60687-728-01" National Drug Code (NDC)

Diltiazem Hydrochloride 100 BLISTER PACK in 1 CARTON (60687-728-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-728-11)
(American Health Packaging)

NDC Code60687-728-01
Package Description100 BLISTER PACK in 1 CARTON (60687-728-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-728-11)
Product NDC60687-728
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20231201
Marketing Category NameANDA
Application NumberANDA074185
ManufacturerAmerican Health Packaging
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]

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