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"59762-0702-3" National Drug Code (NDC)
Mycophenolate Mofetil 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59762-0702-3)
(Greenstone LLC)
NDC Code
59762-0702-3
Package Description
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59762-0702-3)
Product NDC
59762-0702
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Mycophenolate Mofetil
Non-Proprietary Name
Mycophenolate Mofetil
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20100611
Marketing Category Name
ANDA
Application Number
ANDA090456
Manufacturer
Greenstone LLC
Substance Name
MYCOPHENOLATE MOFETIL
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Antimetabolite Immunosuppressant [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59762-0702-3