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"69367-122-07" National Drug Code (NDC)

Hydrochlorothiazide 1000 mg in 1 BOTTLE (69367-122-07)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-122-07
Package Description1000 mg in 1 BOTTLE (69367-122-07)
Product NDC69367-122
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20160201
Marketing Category NameANDA
Application NumberANDA203018
ManufacturerWestminster Pharmaceuticals, LLC
Substance NameHYDROCHLOROTHIAZIDE
Strength25
Strength Unitmg/25mg
Pharmacy ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69367-122-07





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