"53808-0436-1" National Drug Code (NDC)

Ibuprofen 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0436-1)
(State of Florida DOH Central Pharmacy)

NDC Code53808-0436-1
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0436-1)
Product NDC53808-0436
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090701
Marketing Category NameANDA
Application NumberANDA071335
ManufacturerState of Florida DOH Central Pharmacy
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

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