"21130-921-14" National Drug Code (NDC)

Ibuprofen 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21130-921-14)
(Better Living Brands, LLC)

NDC Code21130-921-14
Package Description500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21130-921-14)
Product NDC21130-921
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19880524
Marketing Category NameANDA
Application NumberANDA075010
ManufacturerBetter Living Brands, LLC
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1

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