"16571-742-42" National Drug Code (NDC)

Lansoprazole 3 BOTTLE in 1 CARTON (16571-742-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
(Rising Pharma Holdings, Inc.)

NDC Code16571-742-42
Package Description3 BOTTLE in 1 CARTON (16571-742-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product NDC16571-742
Product Type NameHUMAN OTC DRUG
Proprietary NameLansoprazole
Non-Proprietary NameLansoprazole
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20210528
Marketing Category NameANDA
Application NumberANDA203306
ManufacturerRising Pharma Holdings, Inc.
Substance NameLANSOPRAZOLE
Strength15
Strength Unitmg/1
Pharmacy ClassesInhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

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