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"68462-209-01" National Drug Code (NDC)

Moexipril Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (68462-209-01)
(Glenmark Pharmaceuticals Inc., USA)

NDC Code68462-209-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (68462-209-01)
Product NDC68462-209
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMoexipril Hydrochloride
Non-Proprietary NameMoexipril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20101231
Marketing Category NameANDA
Application NumberANDA090416
ManufacturerGlenmark Pharmaceuticals Inc., USA
Substance NameMOEXIPRIL HYDROCHLORIDE
Strength7.5
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68462-209-01





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