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"61919-752-30" National Drug Code (NDC)

Meclizine Hydrochloride 30 TABLET in 1 BOTTLE (61919-752-30)
(DirectRX)

NDC Code61919-752-30
Package Description30 TABLET in 1 BOTTLE (61919-752-30)
Product NDC61919-752
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMeclizine Hydrochloride
Non-Proprietary NameMeclizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA200294
ManufacturerDirectRX
Substance NameMECLIZINE HYDROCHLORIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesAntiemetic [EPC],Emesis Suppression [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-752-30





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