www.ndcvalidator.com
National Drug Code Lookup
|
NDC Directory
|
About
|
Feedback
"67877-225-38" National Drug Code (NDC)
Mycophenolate Mofetil 10 BLISTER PACK in 1 CARTON (67877-225-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Ascend Laboratories, LLC)
NDC Code
67877-225-38
Package Description
10 BLISTER PACK in 1 CARTON (67877-225-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
67877-225
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
20111128
Marketing Category Name
ANDA
Application Number
ANDA091249
Manufacturer
Ascend Laboratories, 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/67877-225-38