"21130-292-08" National Drug Code (NDC)

Ibuprofen 1 BOTTLE in 1 CARTON (21130-292-08) > 24 TABLET, FILM COATED in 1 BOTTLE
(Better Living Brands, LLC)

NDC Code21130-292-08
Package Description1 BOTTLE in 1 CARTON (21130-292-08) > 24 TABLET, FILM COATED in 1 BOTTLE
Product NDC21130-292
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19880524
End Marketing Date20190912
Marketing Category NameANDA
Application NumberANDA075010
ManufacturerBetter Living Brands, LLC
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1

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