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"71335-3135-1" National Drug Code (NDC)

Diltiazem Hydrochloride 30 TABLET in 1 BOTTLE (71335-3135-1)
(Bryant Ranch Prepack)

NDC Code71335-3135-1
Package Description30 TABLET in 1 BOTTLE (71335-3135-1)
Product NDC71335-3135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20220926
Marketing Category NameANDA
Application NumberANDA216521
ManufacturerBryant Ranch Prepack
Substance NameDILTIAZEM HYDROCHLORIDE
Strength90
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-3135-1





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