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"21130-921-03" National Drug Code (NDC)

Ibuprofen 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21130-921-03)
(Better Living Brands, LLC)

NDC Code21130-921-03
Package Description10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21130-921-03)
Product NDC21130-921
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19880524
End Marketing Date20241214
Marketing Category NameANDA
Application NumberANDA075010
ManufacturerBetter Living Brands, LLC
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1
Pharmacy ClassesAnti-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/21130-921-03





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