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"71335-2137-1" National Drug Code (NDC)

Meclizine Hydrochloride 30 TABLET in 1 BOTTLE (71335-2137-1)
(Bryant Ranch Prepack)

NDC Code71335-2137-1
Package Description30 TABLET in 1 BOTTLE (71335-2137-1)
Product NDC71335-2137
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMeclizine Hydrochloride
Non-Proprietary NameMeclizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20211227
End Marketing Date20241031
Marketing Category NameANDA
Application NumberANDA084657
ManufacturerBryant Ranch Prepack
Substance NameMECLIZINE HYDROCHLORIDE
Strength12.5
Strength Unitmg/1
Pharmacy ClassesAntiemetic [EPC], Emesis Suppression [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2137-1





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