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"72189-231-21" National Drug Code (NDC)
Ibuprofen 21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)
(DIRECT RX)
NDC Code
72189-231-21
Package Description
21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)
Product NDC
72189-231
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ibuprofen
Non-Proprietary Name
Ibuprofen
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210604
Marketing Category Name
ANDA
Application Number
ANDA090796
Manufacturer
DIRECT RX
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/72189-231-21