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"70882-117-21" National Drug Code (NDC)
Prednisone 21 TABLET in 1 BLISTER PACK (70882-117-21)
(Cambridge Therapeutics Technologies, LLC)
NDC Code
70882-117-21
Package Description
21 TABLET in 1 BLISTER PACK (70882-117-21)
Product NDC
70882-117
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Prednisone
Non-Proprietary Name
Prednisone
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20010829
Marketing Category Name
ANDA
Application Number
ANDA040362
Manufacturer
Cambridge Therapeutics Technologies, LLC
Substance Name
PREDNISONE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70882-117-21