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"0093-7771-13" National Drug Code (NDC)

Risedronate Sodium 3 BLISTER PACK in 1 CARTON (0093-7771-13) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7771-19)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7771-13
Package Description3 BLISTER PACK in 1 CARTON (0093-7771-13) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-7771-19)
Product NDC0093-7771
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRisedronate Sodium
Non-Proprietary NameRisedronate Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20161128
Marketing Category NameANDA
Application NumberANDA079215
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameRISEDRONATE SODIUM MONOHYDRATE
Strength150
Strength Unitmg/1
Pharmacy ClassesBisphosphonate [EPC], Diphosphonates [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7771-13





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