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"72579-015-04" National Drug Code (NDC)

Beqalzi 1 KIT in 1 KIT (72579-015-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-017-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-025-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-022-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-020-04)
(BeOne Medicines USA, Inc.)

NDC Code72579-015-04
Package Description1 KIT in 1 KIT (72579-015-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-017-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-025-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-022-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK (72579-020-04)
Product NDC72579-015
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBeqalzi
Non-Proprietary NameSonrotoclax
Dosage FormKIT
Start Marketing Date20260831
Marketing Category NameNDA
Application NumberNDA220711
ManufacturerBeOne Medicines USA, Inc.

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72579-015-04





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