"70729-002-50" National Drug Code (NDC)

NDC Code	70729-002-50
Package Description	50 TABLET in 1 BOTTLE (70729-002-50)
Product NDC	70729-002
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Dye Free Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19990301
Marketing Category Name	ANDA
Application Number	ANDA075139
Manufacturer	Breeden Brothers, LLC
Substance Name	IBUPROFEN
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]