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"60687-816-32" National Drug Code (NDC)

Lubiprostone 20 BLISTER PACK in 1 CARTON (60687-816-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-816-33)
(American Health Packaging)

NDC Code60687-816-32
Package Description20 BLISTER PACK in 1 CARTON (60687-816-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-816-33)
Product NDC60687-816
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLubiprostone
Non-Proprietary NameLubiprostone
Dosage FormCAPSULE, GELATIN COATED
UsageORAL
Start Marketing Date20251201
Marketing Category NameANDA
Application NumberANDA209920
ManufacturerAmerican Health Packaging
Substance NameLUBIPROSTONE
Strength8
Strength Unitug/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60687-816-32





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