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"63739-080-10" National Drug Code (NDC)

Diltiazem Hydrochloride 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-080-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(McKesson Corporation dba SKY Packaging)

NDC Code63739-080-10
Package Description10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-080-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC63739-080
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDiltiazem Hydrochloride
Non-Proprietary NameDiltiazem Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19951222
End Marketing Date20210831
Marketing Category NameANDA
Application NumberANDA074185
ManufacturerMcKesson Corporation dba SKY Packaging
Substance NameDILTIAZEM HYDROCHLORIDE
Strength60
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63739-080-10





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