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"67296-1217-2" National Drug Code (NDC)
Ibu 20 TABLET in 1 BOTTLE (67296-1217-2)
(RedPharm Drug, Inc.)
NDC Code
67296-1217-2
Package Description
20 TABLET in 1 BOTTLE (67296-1217-2)
Product NDC
67296-1217
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ibu
Non-Proprietary Name
Ibu
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20081120
Marketing Category Name
ANDA
Application Number
ANDA075682
Manufacturer
RedPharm Drug, Inc.
Substance Name
IBUPROFEN
Strength
400
Strength Unit
mg/1
Pharmacy Classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67296-1217-2