"10135-762-05" National Drug Code (NDC)

Cetirizine Hydrochloride 500 TABLET in 1 BOTTLE (10135-762-05)
(Marlex Pharmaceuticals, Inc)

NDC Code10135-762-05
Package Description500 TABLET in 1 BOTTLE (10135-762-05)
Product NDC10135-762
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20221001
Marketing Category NameANDA
Application NumberANDA077498
ManufacturerMarlex Pharmaceuticals, Inc
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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