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"70518-2666-0" National Drug Code (NDC)

Hydrochlorothiazide 30 TABLET in 1 BLISTER PACK (70518-2666-0)
(REMEDYREPACK INC.)

NDC Code70518-2666-0
Package Description30 TABLET in 1 BLISTER PACK (70518-2666-0)
Product NDC70518-2666
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20200331
Marketing Category NameANDA
Application NumberANDA040702
ManufacturerREMEDYREPACK INC.
Substance NameHYDROCHLOROTHIAZIDE
Strength12.5
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2666-0





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