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"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 Code
16571-742-42
Package Description
3 BOTTLE in 1 CARTON (16571-742-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product NDC
16571-742
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Lansoprazole
Non-Proprietary Name
Lansoprazole
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20210528
Marketing Category Name
ANDA
Application Number
ANDA203306
Manufacturer
Rising Pharma Holdings, Inc.
Substance Name
LANSOPRAZOLE
Strength
15
Strength Unit
mg/1
Pharmacy Classes
Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16571-742-42