"70771-1931-5" National Drug Code (NDC)

Diltiazem Hydrochloride 500 TABLET in 1 BOTTLE (70771-1931-5)
(Zydus Lifesciences Limited)

NDC Code70771-1931-5
Package Description500 TABLET in 1 BOTTLE (70771-1931-5)
Product NDC70771-1931
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20260525
Marketing Category NameANDA
Application NumberANDA219253
ManufacturerZydus Lifesciences Limited
Substance NameDILTIAZEM HYDROCHLORIDE
Strength90
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]

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