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"51079-971-20" National Drug Code (NDC)
Fluoxetine 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-971-20) > 1 CAPSULE in 1 BLISTER PACK (51079-971-01)
(UDL Laboratories, Inc.)
NDC Code
51079-971-20
Package Description
100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-971-20) > 1 CAPSULE in 1 BLISTER PACK (51079-971-01)
Product NDC
51079-971
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fluoxetine
Non-Proprietary Name
Fluoxetine Hydrochloride
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20110711
Marketing Category Name
ANDA
Application Number
ANDA075207
Manufacturer
UDL Laboratories, Inc.
Substance Name
FLUOXETINE HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51079-971-20