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"71205-522-06" National Drug Code (NDC)
Ibuprofen 6 TABLET, FILM COATED in 1 BOTTLE (71205-522-06)
(Proficient Rx LP)
NDC Code
71205-522-06
Package Description
6 TABLET, FILM COATED in 1 BOTTLE (71205-522-06)
Product NDC
71205-522
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ibuprofen
Non-Proprietary Name
Ibuprofen
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20180824
Marketing Category Name
ANDA
Application Number
ANDA078329
Manufacturer
Proficient Rx LP
Substance Name
IBUPROFEN
Strength
600
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/71205-522-06