"69452-191-30" National Drug Code (NDC)

Ivabradine 500 TABLET, FILM COATED in 1 BOTTLE (69452-191-30)
(Bionpharma Inc.)

NDC Code69452-191-30
Package Description500 TABLET, FILM COATED in 1 BOTTLE (69452-191-30)
Product NDC69452-191
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIvabradine
Non-Proprietary NameIvabradine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250301
Marketing Category NameANDA
Application NumberANDA213276
ManufacturerBionpharma Inc.
Substance NameIVABRADINE HYDROCHLORIDE
Strength7.5
Strength Unitmg/1
Pharmacy ClassesHyperpolarization-activated Cyclic Nucleotide-gated Channel Antagonists [MoA], Hyperpolarization-activated Cyclic Nucleotide-gated Channel Blocker [EPC]

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