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"68788-7079-7" National Drug Code (NDC)

Ibuprofen 21 TABLET, FILM COATED in 1 BOTTLE (68788-7079-7)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7079-7
Package Description21 TABLET, FILM COATED in 1 BOTTLE (68788-7079-7)
Product NDC68788-7079
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200617
Marketing Category NameANDA
Application NumberANDA090796
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameIBUPROFEN
Strength800
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/68788-7079-7





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