"61919-429-30" National Drug Code (NDC)

Cetirizine Hydrochloride 30 TABLET in 1 BOTTLE (61919-429-30)
(DIRECT RX)

NDC Code61919-429-30
Package Description30 TABLET in 1 BOTTLE (61919-429-30)
Product NDC61919-429
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20161222
Marketing Category NameANDA
Application NumberANDA077829
ManufacturerDIRECT RX
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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